MEDLINE INDUSTRIES, LP - Northfield 2024-09-04 Health serious FDA
Health · FDA · Recall #FDA-Z-2741-2024
Medline procedural kits labeled as: PREOP NERVE BLOCK TRAY, Pack Number DYNJRA2040H Recall
Issued September 4, 2024 · MEDLINE INDUSTRIES, LP - Northfield
In September 2024, MEDLINE INDUSTRIES, LP - Northfield recalled the Medline procedural kits labeled as: PREOP NERVE BLOCK TRAY, Pack Number DYNJRA2040H, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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.
What you should do
- 1 Stop using Medline procedural kits labeled as: PREOP NERVE BLOCK TRAY, Pack Number DYNJRA2040H right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact MEDLINE INDUSTRIES, LP - Northfield to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- MEDLINE INDUSTRIES, LP - Northfield
- Category
- Health
- Recall date
- September 4, 2024
- Units affected
- Not reported
- Sold at
- Worldwide
- Recall number
- FDA-Z-2741-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- MEDLINE INDUSTRIES, LP - Northfield has 108 recalls in our database, including 12 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.