Medline procedure kits labeled as: 1) ANGIOGRAPHY recall
Medline procedure kits labeled as: 1) ANGIOGRAPHY SPECIALS
Why was Medline procedure kits labeled as: 1) ANGIOGRAPHY 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 DYNJ60655D: UDI/DI 10195327464783 (each), 40195327464784 (case), Lot Number 24AMC692A
- Product
- Medline procedure kits labeled as: 1) ANGIOGRAPHY SPECIALS
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Quantity
- 1152 units
- Distribution
- Worldwide distribution - US Nationwide and the country of Canada.
- Recall date
- April 2, 2025
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)