Sterile Knee Instruments Disposable Fluted Headless recall: Sterility Concern
Sterile Knee Instruments Disposable Fluted Headless Pins, DIA 3.2mm LNTH 89mm, REF 7650-2038A - Product Usage: Howmedica Osteonics Corp. (Stryker…
Why was Sterile Knee Instruments Disposable Fluted Headless recalled?
Potential for outer pouch sterile barrier to be compromised
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 SC22130X Exp 2023-08-05
- Product
- Sterile Knee Instruments Disposable Fluted Headless Pins, DIA 3.2mm LNTH 89mm, REF 7650-2038A - Product Usage: Howmedica Osteonics Corp. (Stryker…
- Recalling firm
- Howmedica Osteonics Corp.
- Quantity
- 15 pouches
- Distribution
- US Nationwide in the states of AL, FL, IL, MI, NJ & OH.
- Recall date
- November 14, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)