Zimmer Biomet, Inc. recalls CPT 12/14 COCR SIZE 0 STD prosthesis, hip, semi-constrai
See all recalls from Zimmer Biomet, Inc. →Recalled Product
CPT 12/14 COCR SIZE 0 STD prosthesis, hip, semi-constrained, metal/polymer, porous uncemented
Hazard / Issue
The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is removed from the bag.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Item Number: 00-8114-000-00 Lot Numbers: 61779346 61783708
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
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