Zimmer Biomet Recalls CER BIOLOXD OPTION HD 32MM Due to Labeling Error
Zimmer Biomet is recalling CER BIOLOXD OPTION HD 32MM implants because the internal patient label may be incorrect, although the outer box and product are correctly identified.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II and involves a labeling error where the product itself is correctly identified, fitting the criteria for minor labeling errors or low-risk issues.
Plain-English summary
Zimmer Biomet, Inc. is recalling CER BIOLOXD OPTION HD 32MM, model # 650-1056, lot number 843260. The recall is due to a possibility that the patient label inside the product box was incorrectly labeled. The outer box label and the actual product are correctly identified, but the internal patient label could be incorrect.
The affected products were distributed nationwide in the US and internationally in Argentina, the Netherlands, and Canada. This recall is classified as Class II by the U.S. Food and Drug Administration.
Healthcare providers and patients should verify the product identification against the outer box label to ensure the correct implant is used. No specific instructions for consumers are provided in the source text beyond the identification of the labeling discrepancy.
The recalled product
- Product
- CER BIOLOXD OPTION HD 32MM, model # 650-1056
- Manufacturer
- Zimmer Biomet, Inc.
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot Number: 843260
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 10 recalled by Zimmer Biomet, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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