Drape 9732722 Tube Sterile O-arm 20pk recall: Sterility Concern
DRAPE 9732722 TUBE STERILE O-ARM 20PK
Why was Drape 9732722 Tube Sterile O-arm 20pk recalled?
Medtronic Navigation is recalling certain Medtronic single-use, disposable devices because there was not sufficient control to assure that returned, unused devices were appropriately examined for product and/or package damage to ensure sterility.
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?
Lot No.: D120065 D121495 D121515 D120175 D122611 D101555
- Product
- DRAPE 9732722 TUBE STERILE O-ARM 20PK
- Recalling firm
- Medtronic Navigation, Inc.
- Quantity
- 26,674 total
- Distribution
- Nationwide Distribution
- Recall date
- November 26, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)