Zimmer Biomet recalls ASI 2.0 Calcar Trimmer Shafts (model 110032331) due to risk of improper mating with Calcar Planar Shaft instruments. Affected units include specific lots.
The potential that the end of the shaft could fail to effectively mate with the broach with the Calcar Planar Shaft instrument, part number 110032331.
Zimmer Biomet is recalling ASI 2.0 Calcar Trimmer Shafts (model 110032331) because they might not fit properly with Calcar Planar Shaft instruments. This could lead to ineffective use during dental procedures. The recall affects specific lots of the product.
The shaft may not connect properly with the Calcar Planar Shaft instrument, which could cause ineffective use during dental procedures. This might lead to improper treatment outcomes but does not pose a direct risk of injury.
Dentists and dental professionals who use Zimmer Biomet ASI 2.0 Calcar Trimmer Shafts (model 110032331) are affected. Those using the product with Calcar Planar Shaft instruments are most at risk.
Check for model number 110032331 on the shaft. Affected units include specific lots: 784060 and 662870.
Look for model number 110032331 on the shaft to confirm if it's affected.
The recall indicates a potential for improper mating with Calcar Planar Shaft instruments, which could lead to ineffective use during dental procedures. It does not pose a direct risk of injury.
Check the model number on the shaft. If it's 110032331 and from affected lots (784060 or 662870), contact Zimmer Biomet for further instructions.
Affected units have model number 110032331 and are from specific lots: 784060 or 662870.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0517-2020 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-0517-2020 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.
