Medline procedure kits labeled as: 1) BILATERAL FACET recall
Medline procedure kits labeled as: 1) BILATERAL FACET TRAY, Pack Number DYNJRA0869A; 2) PAIN MANAGEMENT TRAY-LF, Pack Number DYNJRA1749
Why was Medline procedure kits labeled as: 1) BILATERAL FACET 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.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
1) Pack Number DYNJRA0869A, 10889942531059 (each) 40889942531050 (case), Lot Number 20KBD382A; 2) Pack Number DYNJRA1749, 10193489829273 (each) 40193489829274 (case), Lot Number 24CMF477A
- Product
- Medline procedure kits labeled as: 1) BILATERAL FACET TRAY, Pack Number DYNJRA0869A; 2) PAIN MANAGEMENT TRAY-LF, Pack Number DYNJRA1749
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Quantity
- 340 units
- Distribution
- Worldwide distribution - US Nationwide and the country of Canada.
- Recall date
- April 2, 2025
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)