INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 recall
INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Right
Why was INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 recalled?
Right nails were anodized, marked, and labelled as left nails and vice versa
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?
Product number: 71676627 (DI: 00885556131633), Batch Number: 21LT56988; 71676628 (DI: 00885556040027), Batch number: 21LT56989
- Product
- INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Right
- Recalling firm
- Smith & Nephew Orthopaedics GmbH
- Quantity
- 17 units
- Distribution
- Distributed nationwide to GA, OH, IN, TX, CO, MO, TN, CA, NC, PA and internationally to Canada, Australia.
- Recall date
- June 1, 2022
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)