Zimmer Dental recalls TSVTB11 implant vial caps that may crack during manufacturing. Affected lots include #63519794. Consumers should check UDI codes for details.
Some implant vial caps in the recalled implant lot may inadvertently crack as the result of a manufacturing assembly condition.
Zimmer Dental is recalling Tapered Screw-Vent MT: Model TSVTB11 implant vial caps that may crack due to a manufacturing issue. This could lead to improper sealing of the vial, potentially causing contamination or leakage.
The vial caps may crack during manufacturing, which could lead to improper sealing. This might cause contamination or leakage of the dental implant solution, potentially affecting the safety of the procedure.
Dental professionals using Zimmer Dental's TSVTB11 implant vial caps with lot number #63519794 are affected. Those handling the vials during dental procedures are most at risk.
Check for the lot number #63519794 on the vial cap. The unique device identifier (UDI) is (01)00889024019935 (17)211130 (10)63519794. This product was sold with Zimmer Dental's TSVTB11 model.
Look for the lot number #63519794 on the vial cap to confirm if it is affected.
The vial caps may crack during manufacturing, which could lead to improper sealing and potential contamination or leakage of the dental implant solution.
Check for the lot number #63519794 on the vial cap. The unique device identifier (UDI) is (01)00889024019935 (17)211130 (10)63519794.
The recall record does not specify a remedy, so contact Zimmer Dental directly for further instructions.
We’ve drafted a message you can send Zimmer Dental to request your refund or repair — edit it as you like.
Subject: Recall Z-0284-2018 — Zimmer Dental Zimmer Dental Hello, I own a Zimmer Dental that is covered by recall Z-0284-2018 from Zimmer Dental. 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.