Class II FDA device recall · Z-2714-2024

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.

Medline medical procedure kits labeled as follows: a) ARTHROSCOPY, REF DYNJ909699; b) BACK CDS, REF CDS984000C; c) EXTREMITY, REF DYNJ900847A; d) HAND-LF, REF DYNJ902619G; e) HIP PINNING CDS, REF CDS984009C; f) HIP PINNING/TFN/ANTERIOR HIP, REF DYNJ902380K; g) KNEE, REF DYNJ904771B; h) KNEE ARTHROSCOPY, REF DYNJ905519D; i) KNEE ARTHROSCOPY, REF DYNJ906273F; j) KNEE ARTHROSCOPY, REF DYNJ909747; k) KNEE ARTHROSCOPY V, REF DYNJS2029D; l) LAMINECTOMY, REF DYNJ907159A; m) LOWER EXTREMITY, REF DYNJ904767A; n) LOWER EXTREMITY, REF DYNJ905518F; o) LOWER EXTREMITY, REF DYNJ909938; p) MINOR EXTREMITY, REF DYNJ909939; q) PODIATRY, REF DYNJ906275D; r) SHOULDER, REF DYNJ904769C; s) SHOULDER, REF DYNJ905511D; t) SHOULDER, REF DYNJ909749; u) SHOULDER ARTHROSCOPY, REF DYNJ906274F; v) SHOULDER ARTHROSCOPY CDS, REF CDS984008C; w) SOUTH EXTREMITY, REF DYNJ909212A; x) SPINE, REF DYNJ905512F; y) TOTAL, REF DYNJ909704; z) TOTAL HIP, REF DYNJ907157A; aa) TOTAL HIP BASIC, REF DYNJ902368K; bb) TOTAL JOINT, REF DYNJ905513G; cc) TOTAL JOINT, REF DYNJ908375C; dd) TOTAL JOINT II, REF DYNJS2027F; ee) TOTAL KNEE, REF DYNJ907158A; ff) TOTAL KNEE CDS, REF CDS983991C; gg) TOTAL SHOULDER, REF DYNJ902367J; hh) TURK-HAND, REF DYNJ905852C; ii) UPPER EXTREMITY, REF DYNJ905514D

Why it was recalled

A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.

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

a) REF DYNJ909699, UDI/DI 40195327446759 (case), 10195327446758 (unit), Lot Numbers:  DYNJ909699, DYNJ909699, DYNJ909699, DYNJ909699, DYNJ909699, DYNJ909699;   b) REF CDS984000C, UDI/DI 40889942011552 (case), 10889942011551 (unit), Lot Numbers:  22GBT604, 22IBI040, 23ABA955, 23DBT170, 23EBU747, 23HBB409;   c) REF DYNJ900847A, UDI/DI 40888277771209 (case), 10888277771208 (unit), Lot Numbers:    d) REF DYNJ902619G, UDI/DI 40195327214488 (case), 10195327214487 (unit), Lot Numbers:  22FBG650, 22FBK152, 22FBW287, 22HBA416, 22HBG372, 22HBS529, 22JBA184, 23EBC466, 23HBL953;   e) REF CDS984009C, UDI/DI 40888277768971 (case), 10888277768970 (unit), Lot Numbers:  22FBL426, 22GBU282, 23CBD236, 23HBY917;   f) REF DYNJ902380K, UDI/DI 40195327507009 (case), 10195327507008 (unit), Lot Numbers:  23KBX257;   g) REF DYNJ904771B, UDI/DI 40195327137190 (case), 10195327137199 (unit), Lot Numbers:  22EMB001, 22IMF542, 22KMC063, 23AME421, 23CMC716, 23DME033, 23FMI125, 23HMC273, 23HMI602, 23LME735;   h) REF DYNJ905519D, UDI/DI 40193489967396 (case), 10193489967395 (unit), Lot Numbers:  22GMG221, 22HMB217, 22LMJ233, 23AME962, 23AMI318, 23AMJ640, 23DMI673, 23IMG465, 23LMD163;   i) REF DYNJ906273F, UDI/DI 40195327511013 (case), 10195327511012 (unit), Lot Numbers:  23JBH985;   j) REF DYNJ909747, UDI/DI 40195327468201 (case), 10195327468200 (unit), Lot Numbers: 23HBZ535, 23KBF559;   k) REF DYNJS2029D, UDI/DI 40193489214414 (case), 10193489214413 (unit), Lot Numbers:  22IDA884, 22LDA526, 23CDA885, 23FDA459, 23JDB741;   l) REF DYNJ907159A, UDI/DI 40193489970419 (case), 10193489970418 (unit), Lot Numbers:  22EME489, 22FMH850, 22IMA282, 22JME894, 22LME340, 23AMB899, 23AMB937, 23AMF082, 23AMG074, 23AMJ063, 23BMF089, 23CMA038, 23FMF222, 23GMB990, 23GMF747, 23HMH495, 23JMC384, 23LMD528;   m) REF DYNJ904767A, UDI/DI 40889942850953 (case), 10889942850952 (unit), Lot Numbers:  22EMI503, 22IMC879, 22KMD093, 22LME746, 23AMC120, 23DMA417, 23DMD168, 23FME590, 23GMH321, 23HMG168;   n) REF DYNJ905518F, UDI/DI 40195327040407 (case), 10195327040406 (unit), Lot Numbers:  22FMI412, 22HMD694, 22IMA909, 22JMC316, 22KMC860, 22LMD325, 23AMF318, 23BMG871, 23EMF948, 23FMA357, 23GMD311, 23HMG163, 23JMA417, 23KMB755, 23LME256;   o) REF DYNJ909938, UDI/DI 40195327511228 (case), 10195327511227 (unit), Lot Numbers:  23JBI008;   p) REF DYNJ909939, UDI/DI 40195327511235 (case), 10195327511234 (unit), Lot Numbers:  23JBH778, 23KBU569;   q) REF DYNJ906275D, UDI/DI 40195327510986 (case), 10195327510985 (unit), Lot Numbers:  23JBI291, 23LBO829;   r) REF DYNJ904769C, UDI/DI 40195327137039 (case), 10195327137038 (unit), Lot Numbers:  22FMB469, 22IMA132, 22KMD488, 22LME616, 23GMF950, 23HME593, 23JMG901, 23KMG320;   s) REF DYNJ905511D, UDI/DI 40193489967549 (case), 10193489967548 (unit), Lot Numbers:  DYNJ905511D, DYNJ905511D, DYNJ905511D, DYNJ905511D, DYNJ905511D, DYNJ905511D, DYNJ905511D;   t) REF DYNJ909749, UDI/DI 40195327468225 (case), 10195327468224 (unit), Lot Numbers:  23IBM342;   u) REF DYNJ906274F, UDI/DI 40195327511020 (case), 10195327511029 (unit), Lot Numbers:  23JBQ500, 23LBI456;   v) REF CDS984008C, UDI/DI 40888277768988 (case), 10888277768987 (unit), Lot Numbers:  22GBL020, 22JBE903, 23ABI396, 23ABM540, 23CBO804;   w) REF DYNJ909212A, UDI/DI 40195327493241 (case), 10195327493240 (unit), Lot Numbers:  23JBA160, 23KBA970;   x) REF DYNJ905512F, UDI/DI 40195327225378 (case), 10195327225377 (unit), Lot Numbers:  22JME529, 22KMD611, 22LMI893, 23BMI268, 23CMF328, 23FMG242, 23HMH500, 23IMC073, 23IMG464, 23JMI252, 23LMC546;   y) REF DYNJ909704, UDI/DI 40195327446919 (case), 10195327446918 (unit), Lot Numbers:  23GBN059, 23KBA374;   z) REF DYNJ907157A, UDI/DI 40193489970358 (case), 10193489970357 (unit), Lot Numbers:  22FMD804, 22JMG489, 22LMC517, 23BMA251, 23CMC137, 23CME146, 23DMA129, 23EMF952, 23FMG076, 23GMI555, 23IME182, 23JMI348, 23KMA447;   aa) REF DYNJ902368K, UDI/DI 40195327505890 (case), 10195327505899 (unit), Lot Numbers:  23JBI661, 23KBT583;   bb) REF DYNJ905513G, UDI/DI 40193489968027 (case), 10193489968026 (unit), Lot Numbers:  22FMG260, 22JMB517, 22JMF062, 23BME809, 23BMF391, 23BMG366, 23BMG367, 23BMI412, 23EMB428, 23FMA677, 23GMD648, 23JMC096, 23KMB846, 23LMC515;   cc) REF DYNJ908375C, UDI/DI 40195327484263 (case), 10195327484262 (unit), Lot Numbers:  23IBL834, 23KBD095, 23LBB392;   dd) REF DYNJS2027F, UDI/DI 40195327360314 (case), 10195327360313 (unit), Lot Numbers:  23EDA949, 23GDA203, 23HDB800, 23JDB140, 23KDA685, 23KDC088;   ee) REF DYNJ907158A, UDI/DI 40183489970402 (case), 10195327137038 (unit), Lot Numbers:  22EME052, 22FMG234, 22IMC193, 22IMH124, 22LME781, 23CMD417, 23CME132, 23CMF812, 23DMF106, 23GMB888, 23HMH494, 23IME266, 23JMA733, 23KMH135;   ff) REF CDS983991C, UDI/DI 40889942131410 (case), 10889942131419 (unit), Lot Numbers:  22FBB136, 22FBU282, 22GBN805, 22HBG300, 22HBS717, 22IBI043, 23CBT616, 23EBA215, 23EBU789, 23HBI490;   gg) REF DYNJ902367J, UDI/DI 40195327505838 (case), 10195327505837 (unit), Lot Numbers:  23JBG975, 23KBN775, 23KBP709;   hh) REF DYNJ905852C, UDI/DI 40195327214204 (case), 10195327214203 (unit), Lot Numbers:  22IBK464, 22IBM480, 23ABO113, 23ABO114, 23ABQ791, 23DBP733, 23EBR661, 23GBO389, 23HBX998, 23KBG164, 23LBF311;   ii) REF DYNJ905514D, UDI/DI 40193489968034 (case), 10193489968033 (unit), Lot Numbers:  22EMA529, 22EMH888, 22FMB880, 22GME946, 22GMH574, 22GMI092, 22HMH887, 22LMD324, 22LMI453, 23AMG866, 23IMG780

Recall status

Ongoing — the recall is still being carried out.

Where it was distributed

Worldwide - US Nationwide and the countries of Panama, Mexico, Canada, Qatar, El Salvador, Oman, Colombia, Singapore.

Recall record

Recalling firm: MEDLINE INDUSTRIES, LP - Northfield
Product type: Devices
Recall number: Z-2714-2024
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: 2024-03-22

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-2714-2024 · Source: openFDA enforcement.