Epimed recalls sterile R-F Injector Cannulas with incorrect expiration dates on packaging. Affected units may expire before intended use. Consumers should check expiration dates and contact Epimed for details.
Incorrect expiration date on introduction cannula packaging.
Epimed is recalling sterile R-F Injector Cannulas that have incorrect expiration dates on their packaging. This could lead to using expired products during medical procedures, potentially causing ineffective treatments or safety risks.
The cannulas have incorrect expiration dates printed on their packaging. This means the products might expire before the intended use date, potentially leading to ineffective treatments or safety issues during medical procedures.
Medical professionals using Epimed's R-F Injector Cannulas for radiofrequency pain procedures are most at risk. Patients receiving these cannulas may also be affected if the expiration date is incorrect.
Check for the product code 257-1810 or 257-1810D with specific sterile lot numbers and expiration dates listed in the description. The affected units have expiration dates that may be incorrect on the packaging.
Verify the expiration date on the packaging against the listed dates (e.g., 3-29-23, 1-21-24).
The Epimed R-F Injector Cannulas have incorrect expiration dates on their packaging, which could lead to using expired products during medical procedures.
Check the expiration date on the packaging and contact Epimed for further instructions.
Yes, the affected models include 257-1810 with sterile lot numbers 14108679 (exp. 3-29-23), 14109199 (exp. 1-21-24), and 14108568 (exp. 2-4-23), and 257-1810D with lot numbers 14109199 (exp. 1-21-24) and 14109690 (exp. 9-26-24).
We’ve drafted a message you can send Epimed to request your refund or repair — edit it as you like.
Subject: Recall Z-1849-2020 — Epimed Epimed Hello, I own a Epimed that is covered by recall Z-1849-2020 from Epimed. 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.
