Folsom Metal Products recalls DKS Disposable Kerrison System (DKS-63030) that were inadvertently distributed for commercial use instead of intended medical use. No action needed as units were not assigned lot numbers.
Units were not intended for commercial distribution and inadvertently distributed.
Folsom Metal Products recalled DKS Disposable Kerrison System instrument sets (DKS-63030) that were mistakenly distributed for commercial use instead of medical use. These items were not intended for sale to the public and were not assigned lot numbers, so no action is required.
These instrument sets were distributed by mistake for commercial use instead of medical use. They were not assigned lot numbers because they were not sent to sterilization, meaning they were not intended for sale to the public.
Medical professionals who received these instrument sets for commercial distribution may have been affected. Patients or others using these items in medical procedures are not at risk as the units were not intended for commercial sale.
Check for the catalog number DKS-63030 with lot numbers 1560, 1567, or 1578. Units without lot numbers were not sent to sterilization and were not intended for commercial distribution.
Look for lot numbers 1560, 1567, or 1578 on the instrument sets.
No action is needed as these units were not intended for commercial distribution and were not assigned lot numbers.
The catalog number is DKS-63030.
These instruments were not intended for commercial use, so they are not safe for general use. However, no action is required as they were not assigned lot numbers.
We’ve drafted a message you can send Folsom Metal Products to request your refund or repair — edit it as you like.
Subject: Recall Z-0650-2025 — Folsom Metal Products Folsom Metal Products Hello, I own a Folsom Metal Products that is covered by recall Z-0650-2025 from Folsom Metal Products. 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.
