Zimmer Biomet recalls Connecting Bolt Model 14-442093 due to potential decrease in fatigue strength leading to fracture. Affected users should contact the company for details.
Product was manufactured from the incorrect material, which shows a potential decrease in the fatigue strength of the connecting bolt that can lead to fracture.
Zimmer Biomet is recalling a specific connecting bolt model because it was made from incorrect material that could weaken over time and cause it to break. This poses a risk of failure during use, which could lead to injury or equipment damage.
The connecting bolt was manufactured from the wrong material, which reduces its ability to withstand repeated stress. This can cause the bolt to fracture over time, potentially leading to equipment failure or injury.
Users of the connecting bolt model 14-442093 are likely affected. Those using this bolt in medical implants or surgical equipment are at higher risk due to potential failure.
Check if you own the Connecting Bolt Model 14-442093. This product was sold by Zimmer Biomet, Inc. and is used in medical implants or surgical equipment.
Reach out to Zimmer Biomet, Inc. for specific instructions on how to address the recall.
The bolt was manufactured from the incorrect material, which shows a potential decrease in fatigue strength and can lead to fracture.
Check for the model number 14-442093 on the product. This bolt is used in medical implants or surgical equipment.
Contact Zimmer Biomet, Inc. for specific instructions on how to address the recall.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-2875-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-2875-2018 from Zimmer Biomet. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
