Medline procedure kits labeled as: 1) C SECTION recall
Medline procedure kits labeled as: 1) C SECTION, Pack Number DYNJ909098
Why was Medline procedure kits labeled as: 1) C SECTION 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) 10195327273132 (each) 40195327273133 (case), Lot Number 23GBK039Z
- Product
- Medline procedure kits labeled as: 1) C SECTION, Pack Number DYNJ909098
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Quantity
- 456 kits
- Distribution
- Worldwide - US Nationwide and the country of Canada.
- Recall date
- March 26, 2025
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)