Percutaneous Gastrojejunostomy Set Product Usage recall
Percutaneous Gastrojejunostomy Set Product Usage: Intended for the percutaneous placement of a catheter for gastroenteric feeding
Why was Percutaneous Gastrojejunostomy Set Product Usage recalled?
Cook has identified that the affected lots may contain wire guides that were loaded backwards into the wire guide holder.
What should I do if I have this product?
Review the official FDA enforcement record for current 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?
WOGS-1200-WH- 050493 Lot number: NS7587941
- Product
- Percutaneous Gastrojejunostomy Set Product Usage: Intended for the percutaneous placement of a catheter for gastroenteric feeding
- Recalling firm
- Cook Inc.
- Quantity
- Quantities co-mingled into line 1
- Distribution
- US Nationwide Distribution
- Recall date
- March 7, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)