Diamatrix recalls Protekt Sharps Safety Knives with incorrect handle size labels (2.5mm shown vs actual 2.2mm). This may cause confusion but does not pose a safety risk. Affected units have specific model and lot numbers.
Surgical knives may contain incorrect description printed on handles. Specifically, some surgical knife handles may contain a size of "2.5mm" when the actual size is "2.2mm".
Diamatrix is recalling Protekt Sharps Safety Knives that have incorrect size labels on the handles. Some knives show a 2.5mm slit when they are actually 2.2mm. This labeling error could cause confusion but does not create a safety hazard.
The knives have a labeling error where the handle shows a 2.5mm slit size but the actual size is 2.2mm. This discrepancy could lead to confusion about the knife's specifications, but it does not cause physical harm or injury.
Users of Protekt Sharps Safety Knives with model REF: PG 44620MU and lot number B923LUC are affected. Medical professionals and surgical staff who use these knives are most at risk due to potential confusion.
Check for the model REF: PG 44620MU and lot number B923LUC on the packaging or individual labels. The handle label may show "2.5mm slit double bevel" instead of the correct 2.2mm.
Verify the handle label for the correct size (2.2mm) and compare with the model number and lot number.
No, the labeling error does not cause physical harm or injury. It only creates confusion about the knife's size.
Model REF: PG 44620MU and lot number B923LUC.
Look for the handle label showing "2.5mm slit double bevel" with model number PG 44620MU and lot number B923LUC.
We’ve drafted a message you can send Diamatrix to request your refund or repair — edit it as you like.
Subject: Recall Z-1120-2022 — Diamatrix Diamatrix Hello, I own a Diamatrix that is covered by recall Z-1120-2022 from Diamatrix. 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.
