Reason for Recall
The mix up of the impression caps provided in the package
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The provided impression caps are magenta instead of brown.
Recall NumberZ-1337-2026ClassificationClass IIIStatusOngoingCategorydeviceInitiated2026-01-06Reported2026-02-18DistributionUS Nationwide distribution.Code InfoArticle Number: 065.4810; UDI-DI: 07630031741110; Lot numbers: VWPX4, VWPX6;Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.