Stryker recalls disposable Spetzler-Malis bipolar forceps with incorrect 54-month shelf life label instead of 36 months. Affected items have specific catalog numbers and lot numbers. Consumers should check labels for expiration date discrepancies.
An error was identified on the expiration date of the product label. The shelf life for the products impacted is 36 months (3 years) however the product label represents a 54 month (4.5 year) shelf life.
Stryker is recalling disposable Spetzler-Malis bipolar forceps that have an incorrect expiration date on their labels. The product is labeled as having a 54-month shelf life when it should only last 36 months. This could lead to using expired products that may not be safe for medical procedures.
The product label incorrectly states a 54-month shelf life instead of the actual 36-month shelf life. This means the instruments could expire earlier than intended, potentially affecting their safety and effectiveness during medical procedures.
Healthcare professionals who use these disposable surgical instruments are most likely affected. The risk is low as the hazard is a labeling error rather than a physical defect.
Check the product label for the catalog number 6760-230-005 and lot numbers 200507007, 200515006, or 201203014. The product is a disposable Spetzler-Malis bipolar forceps with a 23cm length and 0.5mm tip.
Verify the product label shows the correct 36-month shelf life instead of the 54-month label.
The product label incorrectly states a 54-month shelf life instead of the 36-month shelf life, which could lead to using expired instruments.
Check the product label for the correct shelf life. If the label shows 54 months, it is affected and should be checked for use.
The official recall does not provide a fix; the remedy is not stated in the record.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0242-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0242-2024 from Stryker. 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.
