Class II FDA device recall · Z-1437-2024

Class II — the FDA judged the product may cause temporary or medically reversible harm, with a remote chance of serious harm.

This is the FDA's risk judgment for this recall. It describes the potential of the product as a category — it does not establish that any specific unit harmed anyone. Most recalls are Class II or III.

Centurion Forcep kits labeled as: a) STERILE F/P SPLINTER FORCEP (SF6141), Product Code 66165; b) STERILE WEBSTER NEEDLEHOLDER, Product Code 66185; c) STERILE ADSON FORCEP SERR (598), Product Code 66195; d) STERILE DRESSING FORCEP SERR (DF6003), Product Code 66200; e) STERILE TISSUE FORCEP W/TEETH (TF6015), Product Code 66205; f) STERILE F/P WEBSTER NEEDLEHOLDER FN8064, Product Code 66220; g) STERILE IRIS FORCEP W/TEETH (IF250), Product Code 66275; h) STERILE TUBE CLAMP (TOC500), Product Code 66280; i) STERILE F/P SATIN NEEDLEHOLDER (FN9050S), Product Code 66355; j) STERILE 9 1/2 SPONGE FORCEP (237), Product Code 66360; k) STERILE SATIN NEEDLEHOLDER (FN6060S), Product Code 66375; l) STERILE CURV CRILE FORCEP (CF81810), Product Code 66395; m) STERILE LUCAE FORCEP (BF212), Product Code 66415; n) STERILE 6" SF MAYO NEEDLEHOLDER P/S, Product Code 66430; o) STERILE SATIN FORCEP W/TEETH (AF058S), Product Code 66440; p) STERILE 6" FACIAL NEEDLEHOLDER (FN7070S), Product Code 66470; q) STERILE BAYONET FORCEP (25695), Product Code 66490; r) STERILE WEBSTER NEEDLEHOLDER (WN8080S), Product Code 66500; s) STERILE O-H NEEDLEHOLDER (OHN7098S), Product Code 66510; t) STERILE FEILCHENFELD FORCEP (FS388), Product Code 66515; u) STERILE JEWELERS FORCEP (EA742), Product Code 66560; v) STERILE SATIN IRIS FORCEP W/TEETH IF250S, Product Code 66570; w) STERILE CURV PEAN FORCEP (81890), Product Code 66595; x) STERILE CURV 9-1/2 SPONGE FORCEP (FS950), Product Code 66605; y) STERILE SF MAYO HEGAR NDLHLDR (ST263), Product Code 66655; z) STERILE 6" DRESSING FORCEP (DF6006), Product Code 66755; aa) STERILE MAGILL FORCEP (MAGF9), Product Code 66790; bb) STERILE 7 1/4" TUBE OCCLUDING FORCEP, Product Code 66830; cc) STERILE BAUMGARTNER NEEDLEHOLDER, Product Code 66860; dd) STERILE SATIN IRIS FORCEP CVD. (IF255S), Product Code 66865; ee) STERILE ADSON FORCEP W/TYING PLATFORM, Product Code 66970; ff) ST. WEBSTER NEEDLEHOLDER/LG FINGER LOOPS, Product Code 66975; gg) STERILE CVD IRIS FORCEP (ITF4), Product Code 67005; hh) STERILE FULL CURVED IRIS FORCEP (IF145), Product Code 67015; ii) STERILE UMBILICAL LIL'TIPS FORCEP IF145U, Product Code 67060; jj) STERILE SATIN NEEDLEHOLDER (FN6060SL), Product Code 67115; kk) STERILE SCHNIDT TONSIL FORCEP, Product Code 67170; ll) STERILE BISHOP HARMON FORCEP, Product Code 67175; mm) STERILE MAYO HEGAR NEEDLEHOLDER 8"(16290, Product Code 67260; nn) STERILE UTERINE FORCEP 10" (82810), Product Code 67310; oo) STERILE 8" STR PEAN FORCEP (PF12202), Product Code 67485; pp) STERILE MICRO ADSON FORCEP (AF50MS), Product Code 67505; qq) STERILE ADSON FORCEP MICRO TIP (498MS), Product Code 67560; rr) STERILE PLASTIC FORCEP (BF44), Product Code 67590; ss) STERILE MIXTER FORCEP 5 1/2 (12225), Product Code 67700; tt) STERILE TISSUE FORCEP 8"(TF8000), Product Code 67720; uu) STERILE UMBILICAL FORCEP 1/4 CURVE(IF225, Product Code 67725; vv) STERILE DEBAKEY ATRAUMA FORCEP 8"(22546), Product Code 67740; ww) ST PAS GRADE NEEDLEHOLDER 8"(MHN8PAS), Product Code 67865; xx) ST OR MAYO HEGAR NEEDLEHOLDER 6"(OR2500), Product Code 67870; yy) ST OR GRADE WEBSTER N/HOLDER 5"(OR2200), Product Code 67875; zz) ST.MICRO FORCEP 1/4 CRV SER TIP(MC250), Product Code 67885; aaa) STL IRIS FCP 3 1/2" X-FN ANG TP (IFC35FS, Product Code 67910; bbb) STL IRIS FRCP 3 1/2"X-FN STR TP (IFS35FS, Product Code 67915; ccc) STL ADSON FORCEP SMOOTH TIP (598P), Product Code 67925; ddd) ST.HARTMAN EAR DRESSING FORCEP (AF25714), Product Code 67940; eee) STERILE MAYO HEGAR NEEDLEHOLDER, Product Code 67945; fff) STERILE DRESSING FORCEP SERR (DF6003K), Product Code 66200K; ggg) SPONGE FORCEP STRA 9.5" REPRO STERILE, Product Code 66360K; hhh) STERILE 6" SF MAYO NDL HOLDER REPROCESS, Product Code 66430K; iii) STERILE UTERINE FORCEP 10" REPROCESS, Product Code 67310K; jjj) ST CRILE FORCEP,STR 5 1/2" SERR (SC8042), Product Code I67455; kkk) ST. HALSEY NHLDER 5",PAS QLTY TCI (P/S), Product Code I67975; lll) STR. ALLIGATOR M

Why it was recalled

Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.

Is your unit affected?

The recall covers only the specific lots or serial numbers the FDA listed. Enter the lot or serial number from your product's label and we'll check it against that list.

A match means your unit may be covered — stop and call your pharmacist before doing anything. No match suggests it isn't covered, but confirm anyway: code formats vary and lists can be incomplete. Your unit not being listed does not guarantee it is safe, and being listed does not mean you have been harmed.

Show the FDA's listed lot / code information

Centurion:   a) 66165, UDI/DI 60653160018334 (case) 00653160018332 (each), Lot Numbers:  2023111790;   b) 66185, UDI/DI 60653160004887 (case) 00653160004885 (each), Lot Numbers:  2023041090, 2023072590, 2023120190;   c) 66195, UDI/DI 60653160006638 (case) 00653160006636 (each), Lot Numbers: 2023042090, 2023053090, 2023090890, 2023111790;    d) 66200, UDI/DI 60653160022607 (case) 00653160022605 (each), Lot Numbers:  2023020890;   e) 66205, UDI/DI 60653160031944 (case) 00653160031942 (each), Lot Numbers:  2023030390;   f) 66220, UDI/DI 60653160024809 (case) 00653160024807 (each), Lot Numbers:  2023111490;   g) 66275, UDI/DI 60653160038882 (case) 00653160038880 (each), Lot Numbers:  2023060690;   h) 66280, UDI/DI 60653160004870 (case) 00653160004878 (each), Lot Numbers:  2023113090;   i) 66355, UDI/DI 60653160023277 (case) 00653160023275 (each), Lot Numbers:  2023042790;   j) 66360, UDI/DI 50653160022365 (case) 00653160022360 (each), Lot Numbers:  2023032090;   k) 66375, UDI/DI 60653160004856 (case) 00653160004854 (each), Lot Numbers:  2023032790, 2023112990, 2023113090;   l) 66395, UDI/DI 60653160044036 (case) 00653160044034 (each), Lot Numbers:  2023071890;   m) 66415, UDI/DI 60653160018815 (case) 00653160018813 (each), Lot Numbers:  2023041390, 2023101390;   n) 66430, UDI/DI 20653160041211 (case) 00653160041217 (each), Lot Numbers:  2023032390;   o) 66440, UDI/DI 70653160022352 (case) 00653160022353 (each), Lot Numbers:  2023100990, 2023102790;   p) 66470, UDI/DI 10653160039389 (case) 00653160039382 (each), Lot Numbers:  2023070390;   q) 66490, UDI/DI 10653160009030 (case) 00653160009033 (each), Lot Numbers:  2023021690;   r) 66500, UDI/DI 60653160043848 (case) 00653160043846 (each), Lot Numbers:  2023031090;   s) 66510, UDI/DI 10653160050520 (case) 00653160050523 (each), Lot Numbers:  2023071290;   t) 66515, UDI/DI 60653160040953 (case) 00653160040951 (each), Lot Numbers:  2023041090, 2023071290, 2023111590;   u) 66560, UDI/DI 60653160018310 (case) 00653160018318 (each), Lot Numbers:  2023032090, 2023042490, 2023100390;   v) 66570, UDI/DI 60653160038295 (case) 00653160038293 (each), Lot Numbers:  2023041890, 2023060790, 2023071990, 2023101390;   w) 66595, UDI/DI 60653160038127 (case) 00653160038125 (each), Lot Numbers:  2023110890;   x) 66605, UDI/DI 50653160006570 (case) 00653160006575 (each), Lot Numbers:  2023021390, 2023021690;   y) 66655, UDI/DI 50653160011123 (case) 00653160011128 (each), Lot Numbers:  2023101790;   z) 66755, UDI/DI 60653160031401 (case) 00653160031409 (each), Lot Numbers:  2023102690, 2023111390;   aa) 66790, UDI/DI 50653160007676 (case) 00653160007671 (each), Lot Numbers:  2023021090, 2023110290;   bb) 66830, UDI/DI 50653160042042 (case) 00653160042047 (each), Lot Numbers:  2023111490;   cc) 66860, UDI/DI 10653160051268 (case) 00653160051261 (each), Lot Numbers:  2023021490, 2023032990;   dd) 66865, UDI/DI 70653160040844 (case) 00653160040845 (each), Lot Numbers:  2023051990;   ee) 66970, UDI/DI 60653160018792 (case) 00653160018790 (each), Lot Numbers:  2023033090, 2023072090, 2023100590;   ff) 66975, UDI/DI 60653160026032 (case) 00653160026030 (each), Lot Numbers:  2023101290;   gg) 67005, UDI/DI 10653160107415 (case) 00653160107418 (each), Lot Numbers:  2023100690;   hh) 67015, UDI/DI 60653160007147 (case) 00653160007145 (each), Lot Numbers:  2023052290, 2023112190;   ii) 67060, UDI/DI 10653160239338 (case) 00653160061697 (each), Lot Numbers:  2023041490, 2023041790;   jj) 67115, UDI/DI 60653160006683 (case) 00653160006681 (each), Lot Numbers:  2023042490;   kk) 67170, UDI/DI 10653160021360 (case) 00653160021363 (each), Lot Numbers:  2023072690;   ll) 67175, UDI/DI 40653160101575 (case) 00653160101577 (each), Lot Numbers:  2023050890;   mm) 67260, UDI/DI 50653160062330 (case) 00653160062335 (each), Lot Numbers:  2023032790;   nn) 67310, UDI/DI 10653160103264 (case) 00653160103267 (each), Lot Numbers:  2023030390;   oo) 67485, UDI/DI 10653160140924 (case) 00653160140927 (each), Lot Numbers:  2023042590, 2023101990;   pp) 67505, UDI/DI 10653160146568 (case) 00653160146561 (each), Lot Numbers:  2023072090;   qq) 67560, UDI/DI 10653160167877 (case) 00653160167870 (each), Lot Numbers:  2023100390;   rr) 67590, UDI/DI 30653160183017 (case) 00653160183016 (each), Lot Numbers:  2023050890;   ss) 67700, UDI/DI 30653160195898 (case) 00653160195897 (each), Lot Numbers:  2023061290, 2023071090;   tt) 67720, UDI/DI 10653160196068 (case) 00653160196061 (each), Lot Numbers:  2023042590;   uu) 67725, UDI/DI 10653160195931 (case) 00653160195934 (each), Lot Numbers:  2023032790;   vv) 67740, UDI/DI 10653160196099 (case) 00653160196092 (each), Lot Numbers:  2023102790;   ww) 67865, UDI/DI 10653160196839 (case) 00653160196832 (each), Lot Numbers:  2023042490;   xx) 67870, UDI/DI 30653160196895 (case) 00653160196894 (each), Lot Numbers:  2023032790;   yy) 67875, UDI/DI 30653160196901 (case) 00653160196900 (each), Lot Numbers:  2023042790;   zz) 67885, UDI/DI 30653160197861 (case) 00653160197860 (each), Lot Numbers:  2023022290;   aaa) 67910, UDI/DI 10653160202059 (case) 00653160202052 (each), Lot Numbers:  2023051990, 2023060690, 2023062090;   bbb) 67915, UDI/DI 30653160202060 (case) 00653160202069 (each), Lot Numbers:  2023050590;   ccc) 67925, UDI/DI 30653160206914 (case) 00653160206913 (each), Lot Numbers:  2023112790;   ddd) 67940, UDI/DI 10653160210177 (case) 00653160210170 (each), Lot Numbers:  2023072790;   eee) 67945, UDI/DI 10653160211150 (case) 00653160211153 (each), Lot Numbers:  2023072690;   fff) 66200K, UDI/DI 10653160164166 (case) 00653160164169 (each), Lot Numbers:  2023042690;   ggg) 66360K, UDI/DI 00653160352801 (case) 10653160352808 (each), Lot Numbers:  2023050490, 2023050890;     hhh) 66430K, UDI/DI 00653160358605 (case) 10653160358602 (each), Lot Numbers:  2023030990, 2023062890;     iii) 67310K, UDI/DI 00653160358612 (case) 10653160358619 (each), Lot Numbers:  2023030990;   jjj) I67455, UDI/DI 00653160257083 (case) 10653160257080 (each), Lot Numbers:  2023061290;   kkk) I67975, UDI/DI 30653160223614 (case) 00653160223613 (each), Lot Numbers:  2023042490;   lll) I68030, UDI/DI 10653160228288 (case) 00653160228281 (each), Lot Numbers:  2023032090;   mmm) I68035, UDI/DI 10653160228417 (case) 00653160228410 (each), Lot Numbers:   2023041090;     nnn) I68255, UDI/DI 00653160268423 (case) 10653160268420 (each), Lot Numbers: 2023061490, 2023081490, 2023101390;   ooo) I68320, UDI/DI 00653160278842 (case) 10653160278849 (each), Lot Numbers:  2023030990;   ppp) I68420, UDI/DI 00653160287707 (case) 10653160287704 (each), Lot Numbers:  2023021090, 2023091890, 2023101990;   qqq) I68435, UDI/DI 00653160289206 (case) 10653160289203 (each), Lot Numbers:  2023041190;   rrr) I68440, UDI/DI 00653160289213 (case) 10653160289210 (each), Lot Numbers:  2023041190;   sss) I86530, UDI/DI 00653160254686 (case) 10653160254683 (each), Lot Numbers:  2023062890;   ttt) P-66200, UDI/DI 60653160022607 (case) 00653160022605 (each), Lot Numbers:  2023120590 (not distributed);   uuu) TRI66525, UDI/DI 00653160317589 (case) 10653160317586 (each), Lot Numbers:  2023042490, 2023062690, 2023091190, 2023102790;   vvv) TRI66575, UDI/DI 00653160317688 (case) 10653160317685 (each), Lot Numbers:  2023102790;     www) TRI66725, UDI/DI 00653160317961 (case) 10653160317968 (each), Lot Numbers:  2023112890;   xxx) TRI66800, UDI/DI 00653160317930 (case) 10653160317937 (each), Lot Numbers: 2023040490;    yyy) TRI66875, UDI/DI 00653160317893 (case) 10653160317890 (each), Lot Numbers:  2023051290;     zzz) TRI66875K, UDI/DI 00653160358599 (case) 10653160358596 (each), Lot Numbers:  2023030990;   aaaa) TRI66950, UDI/DI 00653160317916 (case) 10653160317913 (each), Lot Numbers:  2023060790;    MEDLINE:  a) DYND04009, UDI/DI 20193489191353 (case) 10193489191356 (each), Lot Numbers:  2023102490;   b) DYND04010, UDI/DI 40884389096469 (case) 10884389096468 (each), Lot Numbers:  2023033190, 2023040390, 2023060290, 2023062190, 2023072090, 2023091990, 2023092990, 2023111690;   c) DYNJ04048, UDI/DI 20193489195245 (case) 10193489195248 (each), Lot Numbers:  2023031090, 2023032890, 2023041890, 2023050390, 2023060890, 2023071190, 2023072590, 2023081590, 2023101990, 2023102890, 2023110890, 2023111590, 2023112290, 2023112890;   d) DYNJ04052, UDI/DI 20193489195252 (case) 10193489195255 (each), Lot Numbers:  2023021590, 2023111390

Recall status

Ongoing — the recall is still being carried out.

Where it was distributed

Worldwide distribution - US Nationwide and the countries of Panama, Canada.

Recall record

Recalling firm: MEDLINE INDUSTRIES, LP - Northfield
Product type: Devices
Recall number: Z-1437-2024
Voluntary / mandated: Voluntary: Firm initiated
Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Origin: Northfield, IL
Recall initiated: 2024-02-23

What to do

Check the lot/code above against your product. To confirm this record and read the FDA's full notice, see the FDA recall page. Before changing anything you take or use, ask your pharmacist or prescriber — this page does not tell you to start or stop any drug or device.

Also available: structured data (JSON-LD) · recall record (JSON)

What this is — and is not

A recall is a recorded FDA enforcement action — the FDA logged that a firm is removing or correcting a product. It does not establish that any specific unit harmed anyone, and causation is not established by a recall. The class above is the FDA's risk judgment for the product category, not a finding about your unit. This page informs and compares; it is not medical advice and never tells you to start or stop a drug or device.

To report a problem you experienced, use FDA MedWatch. Verify this record at FDA recalls · Recall Z-1437-2024 · Source: openFDA enforcement.