Reported Sep 4, 2024 · Ongoing
Medline procedural 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 procedural kits labeled as
9 of 9 products
| # | Product as published |
|---|---|
| 1 | BOTOX KIT - CHRONIC MIGRAINE, Pack Number DYKM2000 |
| 2 | BREAST, Pack Number DYNJ902703K |
| 3 | ENT TYMPANOPLASTY PACK-LF , Pack Number DYNJ38988J; 4)FREE FLAP TRAM ADD ON PACK, Pack Number DYNJ82179A |
| 4 | FREE FLAP TRAM ADD ON PACK, Pack Number DYNJ82179AH |
| 5 | JSI-MUSCLE&PLASTICS PACK-LF , Pack Number DYNJ0608555P |
| 6 | OCCULAR PLASTIC, Pack Number DYNJ901206F |
| 7 | OCCULAR PLASTIC PACK, Pack Number CMPJ05506F |
| 8 | OCCULOPLASTIC PACK, Pack Number DYNJ65156 |
| 9 | PLASTIC PACK, Pack Number DYNJ47842C |
- Lot codes and dates
31 of 31 products
Products covered by this recall # Product as published 1 Lot Number: 21FBO406 DYKM2000 2 Lot Number: 22DBI980 DYKM2000 3 Lot Number: 22KBD028 DYKM2000 4 Lot Number: 23JBC148 DYKM2000 5 Lot Number: 24ABL480 DYKM2000 6 Lot Number: 21ABM981 DYKM2000 7 Lot Number: 21BBR866 DYNJ902703K 8 Lot Number: 21FBI191 DYNJ902703K 9 Lot Number: 21FBR340 DYNJ902703K 10 Lot Number: 22OBL867 DYNJ902703K 11 Lot Number: 22DBH342 DYNJ902703K 12 Lot Number: 22DBI420 DYNJ902703K 13 Lot Number: 22FBM439 DYNJ38988J 14 Lot Number: 23JDA299 DYNJ82179A 15 Lot Number: 23JDB728 DYNJ82179AH 16 Lot Number: 23JDB728 DYNJ0608555P 17 Lot Number: 23GMI735 DYNJ0608555P 18 Lot Number: 23KMC310 DYNJ901206F 19 Lot Number: 23IBC085 DYNJ901206F 20 Lot Number: 23LBA443 DYNJ901206F
This recall covers 55 products
The agency filed one notice per product. You are reading one of them; the other 54 are below.
42 more are in the archive.
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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