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 procedure kits, labeled as: 1) ARTHROGRAM TRAY, Pack Number DYNDH1349; 2) ARTHROGRAM TRAY-LF, Pack Number SPEC0400; 3) ARTHROGRAM/LP/MYELOGRAM TRAY, Pack Number PT220; 4) BIOPSY KIT, Pack Number DYNDH1570; 5) BIOPSY TRAY-LF, Pack Number SPEC4380; 6) BMA BX TRAY, Pack Number DYNDH1050A; 7) BREAST BIOPSY TRAY, Pack Number SPEC0130C; 8) CATHETER ON/OFF KIT, Pack Number DT5490B; 9) CDP, INTRODUCER KIT 9F, Pack Number S5078BF09; 10) CHEST TUBE INSERTION TRAY, Pack Number CHT705; 11) CIRCUMCISION TRAY, Pack Number CIT6260; 12) CUSTOM BIOPSY TRAY, Pack Number MNS4815; 13) DELIVERY ACCESSORY KIT, Pack Number MNS6496; 14) DELIVERY PACK, Pack Number MNS2925A; 15) DELIVERY PACK, Pack Number MNS2925B; 16) E. R. LACERATION TRAY, Pack Number DYNDL1187A; 17) FINE LACERATION KIT, Pack Number SUT19360; 18) GENERAL BIOPSY TRAY- LF, Pack Number SPEC0248B; 19) GENERAL UTILITY, Pack Number DYNDA2524; 20) HOLSTON MYELOGRAM PACK, Pack Number DYNDH1227A; 21) HOLSTON MYELOGRAM PACK, Pack Number DYNDH1227B; 22) I-PACK INJECTION KIT WITH DRAPE, Pack Number MNS12150; 23) LACERATION TRAY, Pack Number DYNDL1757; 24) MYELOGRAM TRAY, Pack Number DYNDH1531; 25) OB DELIVERY SET, Pack Number MNS3355; 26) OB DELIVERY TRAY, Pack Number MNS10875; 27) OB DELIVERY TRAY, Pack Number MNS5575; 28) OB DELIVERY TRAY, Pack Number MNS10875A; 29) PICU LINE TRAY, Pack Number DYNDC1960A; 30) PORT ACCESS KIT, Pack Number DYNDC2945; 31) PORT ACCESS TRAY, Pack Number EBSI1241; 32) SINGLE TAP BLOCK TRAY, Pack Number SPEC0156A; 33) STEREO PROCEDURE TRAY, Pack Number DYNDC2859A; 34) SUTURING SET, Pack Number SUT9790; 35) SUTURING SET, Pack Number SUT4020; 36) TRAY,GENERAL UTILITY, Pack Number DYNDL1422A; 37) U.A.C. TRAY, Pack Number UVT125; 38) ULTRASOUND GUIDED PIV KIT, Pack Number MNS9580; 39) VAGINAL DELIVERY TRAY, Pack Number MNS11020; 40) VAGINAL DELIVERY TRAY, Pack Number MNS11020A
Why it was recalled
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
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
DYNDH1349, Lot Number 2019061090; SPEC0400, Lot Number 2022010790; SPEC0400, Lot Number 2022061490; PT220, Lot Number 2020090390; DYNDH1570, Lot Number 2023091390; SPEC4380, Lot Number 2023110890; DYNDH1050A, Lot Number 2019100490; SPEC0130C, Lot Number 2020072090; DT5490B, Lot Number 2022091590; S5078BF09, Lot Number 2022122390; CHT705, Lot Number 2021072990; CIT6260, Lot Number 2022031190; MNS4815, Lot Number 2022042890; MNS6496, Lot Number 2018112690; MNS6496, Lot Number 2019061390; MNS6496, Lot Number 2020040190; MNS6496, Lot Number 2020062290; MNS6496, Lot Number 2020090290; MNS6496, Lot Number 2021072990; MNS6496, Lot Number 2022010790; MNS6496, Lot Number 2022080890; MNS6496, Lot Number 2022122390; MNS6496, Lot Number 2023040690; MNS2925A, Lot Number 2019080690; MNS2925A, Lot Number 2019101190; MNS2925B, Lot Number 2020032090; MNS2925B, Lot Number 2020071690; DYNDL1187A, Lot Number 2019080590; DYNDL1187A, Lot Number 2019100490; SUT19360, Lot Number 2023021090; SPEC0248B, Lot Number 2019041790; DYNDA2524, Lot Number 2019100490; DYNDH1227A, Lot Number 2019061090; DYNDH1227B, Lot Number 2019100490; MNS12150, Lot Number 2021072990; MNS12150, Lot Number 2022031190; DYNDL1757, Lot Number 2019061090; DYNDH1531, Lot Number 2023021090; MNS3355, Lot Number 2019080590; MNS3355, Lot Number 2019100490; MNS3355, Lot Number 2020050890; MNS3355, Lot Number 2020091090; MNS3355, Lot Number 2020113090; MNS3355, Lot Number 2021030890; MNS3355, Lot Number 2021040990; MNS3355, Lot Number 2021052890; MNS3355, Lot Number 2021071590; MNS3355, Lot Number 2021080990; MNS3355, Lot Number 2021122390; MNS3355, Lot Number 2022030790; MNS3355, Lot Number 2022071590; MNS3355, Lot Number 2022080590; MNS3355, Lot Number 2022101490; MNS3355, Lot Number 2023021090; MNS3355, Lot Number 2023053090; MNS3355, Lot Number 2023091390; MNS3355, Lot Number 2023121490; MNS10875, Lot Number 2019031590; MNS5575, Lot Number 2019061090; MNS5575, Lot Number 2020072090; MNS5575, Lot Number 2020081790; MNS10875A, Lot Number 2020081790; MNS10875A, Lot Number 2020090390; MNS5575, Lot Number 2020102390; MNS5575, Lot Number 2021012590; MNS10875A, Lot Number 2021012690; MNS10875A, Lot Number 2021031190; MNS10875A, Lot Number 2021051490; MNS10875A, Lot Number 2021072990; MNS10875A, Lot Number 2021102890; MNS10875A, Lot Number 2022031190; MNS10875A, Lot Number 2022061490; MNS10875A, Lot Number 2022091590; MNS10875A, Lot Number 2023040690; MNS10875A, Lot Number 2023092990; MNS10875A, Lot Number 2023110890; DYNDC1960A, Lot Number 2022010790; DYNDC2945, Lot Number 2023040690; EBSI1241, Lot Number 2021021190; SPEC0156A, Lot Number 2019100490; DYNDC2859A, Lot Number 2020081790; DYNDC2859A, Lot Number 2023053090; SUT9790, Lot Number 2020090390; SUT9790, Lot Number 2020113090; SUT4020, Lot Number 2021051490; SUT4020, Lot Number 2021072990; SUT4020, Lot Number 2022071590; DYNDL1422A, Lot Number 2019061090; UVT125, Lot Number 2023110890; MNS9580, Lot Number 2019100490; MNS9580, Lot Number 2022042890; MNS11020, Lot Number 2018103190; MNS11020, Lot Number 2019012390; MNS11020, Lot Number 2019041790; MNS11020A, Lot Number 2019080690; MNS11020A, Lot Number 2021021190; MNS11020A, Lot Number 2021030390; MNS11020A, Lot Number 2021041690; MNS11020A, Lot Number 2022042890
Recall status
Ongoing — the recall is still being carried out.
Where it was distributed
worldwide
Recall record
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Product type
- Devices
- Recall number
- Z-2772-2024
- 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
- 2024-04-08
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-2772-2024 · Source: openFDA enforcement.