Reported Sep 4, 2024 · Ongoing
Centurion 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?
Centurion procedure kits labeled as
7 of 7 products
| # | Product as published |
|---|---|
| 1 | BIOPSY KIT, Pack Number DYNDA1466A |
| 2 | BIOPSY SKIN/LACERATION TRAY, Pack Number SUT20455 |
| 3 | CHEST TUBE INSERTION TRAY, Pack Number CHT560 |
| 4 | CUSTOM BIOPSY TRAY, Pack Number MNS4815 |
| 5 | PERITONSILLAR ABSCESS TRAY, Pack Number MNS3560 |
| 6 | PRE POST DIALYSIS, Pack Number DYNDC3274 |
| 7 | STEREO PROCEDURE TRAY, Pack Number DYNDC2859A |
- Lot codes and dates
12 of 12 products
Products covered by this recall # Product as published 1 DYNDA1466A, Lot Number 2022040190 2 SUT20455, Lot Number 2022040190 3 CHT560, Lot Number 2021092290 4 MNS4815, Lot Number 2022040190 5 MNS3560, Lot Number 2021021790 6 MNS3560, Lot Number 2021092290 7 MNS3560, Lot Number 2021092890 8 MNS3560, Lot Number 2022040190 9 MNS3560, Lot Number 2022071490 10 MNS3560, Lot Number 2023121290 11 DYNDC3274, Lot Number 2023121290 12 DYNDC2859A, Lot Number 2021092290
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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