Bodycad recalls specific torque limiting adaptors and osteotomy trays due to breakage risk when used counterclockwise or with power tools. Affected items include part #027-203 and specific lot numbers.
There is a risk of breakage of the torque limiting adaptor if used counterclockwise and it must not be used with a power tool due to no test data validating this use.
Bodycad is recalling certain torque limiting adaptors and osteotomy trays because they can break if used counterclockwise or with power tools. This could lead to injury during dental or surgical procedures.
The torque limiting adaptor can break if used counterclockwise, potentially causing injury. It must not be used with power tools because there is no testing to confirm safety in this scenario.
Dentists and surgeons who use Bodycad's Fine Osteotomy Implant system are most at risk. Patients undergoing procedures with these recalled components may also be affected.
Check for part #027-203 (reusable torque limiting adaptor) or specific lot numbers listed in the recall notice. The product is part of the Bodycad Fine Osteotomy Implant system.
Do not use the torque limiting adaptor in counterclockwise direction as it can break.
Do not use the adaptor with power tools as there is no test data validating this use.
The recalled torque limiting adaptor has part number #027-203.
Affected osteotomy trays have lot numbers SB000251, SB000252, SB000253, SB000254, SB000259, SB000261, SB000263, SB000264, SB000272, and SB000273.
No, the adaptor must not be used with power tools due to lack of test data validating this use.
We’ve drafted a message you can send Bodycad to request your refund or repair — edit it as you like.
Subject: Recall Z-0244-2022 — Bodycad Bodycad Hello, I own a Bodycad that is covered by recall Z-0244-2022 from Bodycad. 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.
