Peri-loc Targeter 4.5mm Distal Femur recall
PERI-LOC TARGETER 4.5MM DISTAL FEMUR, HANDLE, LEFT, NON-STERILE - Product Usage: used for adult and pediatric patients, as well as patients with…
Why was Peri-loc Targeter 4.5mm Distal Femur recalled?
The 4.5MM PeriLoc Targeter right hand part was anodized green and was marked as a left-hand 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?
Product Number: 71173400, Lot Number: 16GM20026
- Product
- PERI-LOC TARGETER 4.5MM DISTAL FEMUR, HANDLE, LEFT, NON-STERILE - Product Usage: used for adult and pediatric patients, as well as patients with…
- Recalling firm
- Smith & Nephew, Inc.
- Quantity
- 3 units
- Distribution
- U.S Nationwide including in the states of IN and TN.
- Recall date
- August 19, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)