Zimmer Biomet Recalls Lateral Troch Plate Due to Labeling Error
Zimmer Biomet is recalling Lateral Troch Plate Full Crimp units because the internal patient label may be incorrect, though the product itself is correct.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
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 Lateral Troch Plate Full Crimp - 254mm, model # 350837, lot number 340530. 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 and consult with their surgeon or Zimmer Biomet if there are concerns regarding the internal patient label.
The recalled product
- Product
- Lateral Troch Plate Full Crimp - 254mm, model # 350837
- 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: 340530
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.
See all 10 products in this recall →Related recalls
Same manufacturer · Zimmer Biomet, Inc.
See all →- HighZimmer Biomet Recalls Spinal Rod Cutters Due to Fracture Risk
FDA (Devices) · 2020-12-30
- ModerateZimmer Biomet Recalls Polaris Spinal System Screws for Labeling Update
FDA (Devices) · 2020-12-23
- HighZimmer Biomet Recalls Hip Prosthesis Cups Due to Sterilant Biocompatibility Concerns
FDA (Devices) · 2020-11-11
- HighZimmer Biomet Recalls Hip Prosthesis Components Due to Sterilant Biocompatibility Concerns
FDA (Devices) · 2020-11-11
- HighZimmer Biomet Recalls Hip Prosthesis Component Due to Sterilant Concerns
FDA (Devices) · 2020-11-11
Same hazard · mis labeling
See all →- SevereWhite Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient
FDA (Food) · 2026-10-14
- SevereBetter Bakehouse Recalls Donutful Chocolate Dipped Vanilla Cake Donuts for Undeclared Milk
FDA (Food) · 2026-10-14
- HighFreshPoint Recalls Cranberry Chicken Salad Wedges for Undeclared Egg Allergen
FDA (Food) · 2026-10-14
- HighJ K Patisserie & Bakery LLC Recalls Croissants for Undeclared Egg
FDA (Food) · 2026-10-14
- ModerateHalyard Laparoscopy Comprehensive Pack II Recalled for Latex Content
FDA (Devices) · 2026-10-14
Similar recalls
- ModerateZimmer Recalls Tibial Plates Due to Patient Label Discrepancies
FDA (Devices) · 2012-11-14
- ModerateZimmer Biomet Recalls Orthopedic Plates Due to Labeling Mismatch
FDA (Devices) · 2016-01-20
- ModerateZimmer Recalls Distal Medial Humeral Locking Plates Due to Labeling Error
FDA (Devices) · 2013-09-04
- ModerateZimmer Biomet Recalls M/L Taper Hip Prosthesis Due to Etching Error
FDA (Devices) · 2016-03-16
- HighZimmer Biomet Recalls 75mm Tibial Tray Implants Due to Sizing Error
FDA (Devices) · 2018-06-20
- ModerateNexGen Tibial Plate Recalled for Incorrect Outer Packaging Label
FDA (Devices) · 2023-07-12