OSTEORAPTOR CRVD 2.3 SA UB COBRD BLUE- Absorbable Suture anchor Product Number: 72203290
Class I - DangerousWhat Should You Do?
- Check if you have this product: Batch Numbers: 2012935 2013910 2016229 2017812 2018635 2019990 2021454 2022268 2024711 2025147 2027400 2029394 2030945 2037184 2038460 2038795 2039253 2039444 2045859 2045858 2045860 2045861 2048368 2049884 2048367
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Smith & Nephew, Inc.
- Reason for Recall:
- Product packaging improper or incomplete seal of the pouch surrounding the sterile product may result in a breach of the sterile barrier created by the pouch
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
OSTEORAPTOR CRVD 2.3 SA UB COBRD BLUE- Absorbable Suture anchor Product Number: 72203290
Product Codes/Lot Numbers:
Batch Numbers: 2012935 2013910 2016229 2017812 2018635 2019990 2021454 2022268 2024711 2025147 2027400 2029394 2030945 2037184 2038460 2038795 2039253 2039444 2045859 2045858 2045860 2045861 2048368 2049884 2048367
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0165-2021
Related Recalls
META-TAN LAG/COMPRESSION SCREW KIT 90MM/85MM, REF: 71642690
Smith & Nephew
Integrated Lag/Compression Screw Kit has a compression screw with hexagon socket that may be undersized, which causes the screw to be non-functional, which would require replacement with another adequate size screw, and exchange may exceed 30 minutes.
Sterile barrier breach due to inadequate packaging design that could not hold the geometry of the device.
The Bipolar assembly contains an oversized Retainer Ring.