Zimmer Biomet ASI 2.0 Calcar Trimmer Shaft Recall: Potential Mating Failure
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.
Lower-risk recall
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.
Contact the company
What happened, in plain English
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. Read more at govinfonow.com/recall/67257-zimmer-biomet-asi-2-0-calcar-trimmer-shaft-recall-potential.
Source Summary by GovInfoNow · govinfonow.com/recall/67257-zimmer-biomet-asi-2-0-calcar-trimmer-shaft-recall-potential · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0517-2020
Cite this page
“Zimmer Biomet ASI 2.0 Calcar Trimmer Shaft Recall: Potential Mating Failure.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/67257-zimmer-biomet-asi-2-0-calcar-trimmer-shaft-recall-potential. Based on FDA recall #Z-0517-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0517-2020%22&limit=1).
Why it’s dangerous
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.
Who’s affected
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.
How to tell if you have this one
Check for model number 110032331 on the shaft. Affected units include specific lots: 784060 and 662870.
- Brand
Zimmer Biomet- Category
Medical device
What to do — step by step
Check Model Number
Look for model number 110032331 on the shaft to confirm if it's affected.
Where it went and when
Where it was distributed
Distributed in 11 states, and outside the U.S.
FDA distribution: “CA, IN, MN, NJ, NY, AR, LA, OH, KY, TX, CO (US) CA, CN, NL (International)” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arkansas, California, Colorado, Indiana, Kentucky, Louisiana, Minnesota, New Jersey, New York, Ohio, Texas.
Recall timeline
FDA terminated this recall 13 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-0517-2020 (August 6, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0517-2020 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.