FEMORAL ARTERY PACK-LF. Sterile Procedural Tray recall
FEMORAL ARTERY PACK-LF. Sterile Procedural Tray
Why was FEMORAL ARTERY PACK-LF. Sterile Procedural Tray recalled?
Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
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?
Item Number: DYNJ0826625Q, Case UDI/GTIN: 40193489377942, Unit UDI/GTIN: 10193489377941, Lot Number: 22KMA163, 22JME722
- Product
- FEMORAL ARTERY PACK-LF. Sterile Procedural Tray
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Quantity
- 15 cases (30 units)
- Distribution
- Worldwide distribution - US Nationwide and the countries of Canada, Japan, Mexico, Panama, Turks & Caicos, United Arab Emirates.
- Recall date
- February 15, 2023
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)