Folsom Metal Products recalls 10-pack sterile distraction pins (Rx only) manufactured August 2020-July 2025 due to unvalidated shelf life labeling. Consumers should contact the manufacturer for details.
Labeling includes shelf life that has not been validated.
Folsom Metal Products is recalling 10-pack sterile distraction pins (Rx only) that have unvalidated shelf life labeling. This means the expiration date on the packaging may not be accurate, potentially leading to unsafe use if the pins are used after the expiration date.
The labeling includes a shelf life that hasn't been validated by the manufacturer. This could mean the pins might expire before the labeled date, leading to potential issues if used after expiration.
Medical professionals who use these pins for dental procedures may be affected. Patients receiving these pins under a prescription are at risk if the pins expire before use.
Check for the product name '14 mm Distraction Pin', 10 single packs, and the UDI code 00850014548032. These pins were distributed from August 1, 2020, to July 30, 2025.
Look for the UDI code 00850014548032 on the packaging to confirm if the pins are part of the recall.
The labeling includes a shelf life that has not been validated by the manufacturer, which could lead to potential issues if the pins expire before the labeled date.
Check for the product name '14 mm Distraction Pin', 10 single packs, and the UDI code 00850014548032. These pins were distributed from August 1, 2020, to July 30, 2025.
The recall record does not specify a remedy, so contact Folsom Metal Products directly for further instructions.
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-2579-2025 — Folsom Metal Products Folsom Metal Products Hello, I own a Folsom Metal Products that is covered by recall Z-2579-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
