AbbVie PEG Kit 20 FR recall
AbbVie PEG Kit 20 FR
Why was AbbVie PEG Kit 20 FR recalled?
AbbVie is issuing an urgent field correction notification due to an increased number of reports of disconnections of the AbbVie 20FR PEG tube from the Y-connectors.
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?
AbbVie PEG Kit 20 Fr Product Code 62912-01-16 with lot numbers: 32025245, 32265215, 32335206, 32335336
- Product
- AbbVie PEG Kit 20 FR
- Recalling firm
- AbbVie Inc.
- Quantity
- 541 units
- Distribution
- U.S. consignees located throughout the country and Puerto Rico. Foreign Consignees: Worldwide.
- Recall date
- December 28, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)