Stryker recalls disposable Spetzler-Malis bipolar forceps with incorrect 54-month shelf life label. Products may expire earlier than intended, but no safety risk exists. Consumers should check product labels for correct expiration date.
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 with a labeling error showing a 54-month shelf life instead of the actual 36-month shelf life. This means the products could expire earlier than labeled, but there is no safety risk to users.
The product label incorrectly states a 54-month shelf life when the actual shelf life is 36 months. This could lead to products expiring earlier than intended, but the error does not affect the product's safety or functionality.
Medical professionals who use these disposable surgical instruments are likely affected. The risk is minimal as the error only affects the product's shelf life labeling, not safety.
Check for the product name 'Disposable Spetzler-Malis Bipolar forceps, 20CM IM DISP BAYONET 0.5MM TIP' with catalog number 6770-200-005. Lot numbers 200924012, 201001029, 201022005, and 201029006 are also affected.
Verify the expiration date on the product label matches the actual 36-month shelf life.
No, the labeling error only affects the product's shelf life, not safety.
Check for the product name 'Disposable Spetzler-Malis Bipolar forceps, 20CM IM DISP BAYONET 0.5MM TIP' with catalog number 6770-200-005 and lot numbers 200924012, 201001029, 201022005, or 201029006.
No, the recall does not require returning the product as there is no safety risk.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0248-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0248-2024 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.
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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.
