MEDLINE procedure kits labeled as follows: 1) NEURAXIAL recall
MEDLINE procedure kits labeled as follows: 1) NEURAXIAL KIT, REF PAIN1876A
Why was MEDLINE procedure kits labeled as follows: 1) NEURAXIAL recalled?
The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
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?
Codes: 1) PAIN1876A UDI-DI: 10195327433666 (each) 40195327433667 (case), Lot Number: 23KLA330
- Product
- MEDLINE procedure kits labeled as follows: 1) NEURAXIAL KIT, REF PAIN1876A
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Quantity
- 360 units
- Distribution
- US Nationwide. Bermuda, Canada, Panama, UAE, US Virgin Islands
- Recall date
- December 4, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)