Femoral Nail recall
Femoral Nail, A/R T2 Femur ¿12x360 mm, Product Number 18251236S
Why was Femoral Nail recalled?
The manufacturer has discovered that potentially out-of-specification products may have left the factory. Non-conforming cannulation of the nails may result in reduced component strength and potentially premature nail breakage.
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?
GTIN 04546540199775; Lot code: K081650
- Product
- Femoral Nail, A/R T2 Femur ¿12x360 mm, Product Number 18251236S
- Recalling firm
- Stryker GmbH
- Quantity
- 9
- Distribution
- The products were distributed to the following US states: AL, Co, FL, KY, NC, TN, UT, and WA.
- Recall date
- July 18, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)