Bone Dowell Harvest Tubes recall: Labeling Error
Bone Dowell Harvest Tubes
Why was Bone Dowell Harvest Tubes recalled?
mislabeled as 8mm tube but it is actually 9 mm in size. A 9mm subcomponent was erroneously substituted and etched as 8mm for the actual 8mm subcomponent part.
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?
Part Number: 900738 Lot Number (LN): 889990
- Product
- Bone Dowell Harvest Tubes
- Recalling firm
- Zimmer Biomet, Inc.
- Quantity
- 49
- Distribution
- No US distribution. JAPAN NETHERLANDS SINGAPORE SWITZERLAND
- Recall date
- May 17, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)