Keystone Dental recalls Paltop 1.25mm Hex Drivers (part 60-70102) due to oversized hex features causing difficulty engaging screws. Affected units sold with lot WO-010354.
Paltop Surgical Kits contain 1.25mm Hex Driver(s) which may have a slightly oversized hex driving feature, make it difficult to engage screws and abutments containing the corresponding screw feature
Keystone Dental is recalling Paltop 1.2:5mm Hex Drivers with part number 60-70102 because the hex features might be slightly oversized. This makes it hard to properly attach screws and abutments during dental procedures. The issue doesn't pose a safety risk but could lead to improper connections.
The hex drivers may have a slightly oversized hex feature, making it difficult to engage with screws and abutments. This could lead to improper connections during dental procedures, but does not cause injury or damage to the user.
Dental professionals using Paltop 1.25mm Hex Drivers with part number 60-70102 are likely affected. Those who use these drivers for dental procedures may be at risk of improper screw engagement.
Check for the part number 60-70102 on the Paltop 1.25mm Hex Drivers. Affected units were sold with lot number WO-010354.
Verify the part number on the driver is 60-70102 and the lot number is WO-010354.
No, the recall does not require stopping use. The issue is about difficulty engaging screws, not a safety hazard.
The official notice does not specify a remedy, so no action is required beyond checking the part number and lot number.
The recall states the issue does not cause injury or damage, only difficulty engaging screws.
We’ve drafted a message you can send Keystone Dental to request your refund or repair — edit it as you like.
Subject: Recall Z-1064-2019 — Keystone Dental Keystone Dental Hello, I own a Keystone Dental that is covered by recall Z-1064-2019 from Keystone 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.
