Reported Apr 2, 2025 · Ongoing
Medline procedure kits labeled as
MEDLINE INDUSTRIES, LP - Northfield
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: MEDLINE INDUSTRIES, LP - Northfield · 3 Lakes Dr · Northfield, IL · 60093-2753
Is this the product you have?
Medline procedure kits labeled as
12 of 12 products
| # | Product as published |
|---|---|
| 1 | DELIVERY PACK, Pack Number DYNJ0923016 |
| 2 | DELIVERY PACK-LF, Pack Number DYNJ0968863M |
| 3 | L & D PACK-LF, Pack Number DYNJ0373290N |
| 4 | L&D PACK, Pack Number DYNJ51998A |
| 5 | LABOR & DELIVERY PACK-LF, Pack Number DYNJ0348455P |
| 6 | LABOR AND DELIVERY TRAY-LF, Pack Number DYNJ23054J |
| 7 | OB DELIVERY-LF, Pack Number DYNJ40096F |
| 8 | VAG DELIVERY PACK, Pack Number DYNJ83056 |
| 9 | VAGINAL DELIVERY, Pack Number DYNJ27939D |
| 10 | VAGINAL DELIVERY PACK, Pack Number DYNJ25843C |
| 11 | VAGINAL DELIVERY PACK, Pack Number DYNJ43395 |
| 12 | VAGINAL DELIVERY PACK-LF, Pack Number DYNJ0594115L |
- Lot codes and dates
12 of 12 products
Products covered by this recall # Barcodes Product as published 1 1088994232308140889942323082Lot Number 23IMF426A; 2) Pack Number DYNJ0968863M: UDI/DI 10889942323081 (each) 40889942323082 (case) 2 1019348996737140193489967372Lot Number 21JMG530A; 3) Pack Number DYNJ0373290N: UDI/DI 10193489967371 (each) 40193489967372 (case) 3 1019348992350640193489923507Lot Number 21IMH700A; 4) Pack Number DYNJ51998A: UDI/DI 10193489923506 (each) 40193489923507 (case) 4 1019532743048140195327430482Lot Number 22IBG256Z; 5) Pack Number DYNJ0348455P: UDI/DI 10195327430481 (each) 40195327430482 (case) 5 1019348921564940193489215640Lot Number 23HMC532A; 6) Pack Number DYNJ23054J: UDI/DI 10193489215649 (each) 40193489215640 (case) 6 1019348992309440193489923095Lot Number 22CMB444A; 7) Pack Number DYNJ40096F: UDI/DI 10193489923094 (each) 40193489923095 (case) 7 1019532723441640195327234417Lot Number 23IMF243A; 8) Pack Number DYNJ83056: UDI/DI 10195327234416 (each) 40195327234417 (case) 8 1019532714823240195327148233Lot Number 22JMB827A; 9) Pack Number DYNJ27939D: UDI/DI 10195327148232 (each) 40195327148233 (case) 9 1088994285373140889942853732Lot Number 22LBE104A; 10) Pack Number DYNJ25843C: UDI/DI 10889942853731 (each) 40889942853732 (case) 10 1088827704944440888277049445Lot Number 21EBN038A; 11) Pack Number DYNJ43395: UDI/DI 10888277049444 (each) 40888277049445 (case) 11 1019348938273040193489382731Lot Number 21LMG173A; 12) Pack Number DYNJ0594115L: UDI/DI 10193489382730 (each) 40193489382731 (case) 12 Lot Number 20JKB018A - Amount recalled
- 1958 units
This recall covers 29 products
The agency filed one notice per product. You are reading one of them; the other 28 are below.
16 more are in the archive.
Where it was sold
- Nationwide
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.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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