Stryker recalls disposable Spetzler-Malis bipolar forceps with incorrect 54-month expiration date label; actual shelf life is 36 months. 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 an incorrect expiration date label. The product shows a 54-month shelf life but should only last 36 months. This could lead to using expired medical tools.
The product label incorrectly states a 54-month shelf life when the actual shelf life is 36 months. Using expired medical instruments could lead to reduced effectiveness or potential contamination.
Medical professionals who use these disposable surgical instruments are likely affected. The risk is low as the hazard is a labeling error, not a safety issue.
Check for the product name 'Disposable Spetzler-Malis Bipolar forceps, 18CM IM DISP BAYONET 1.0MM TIP' with catalog number 6770-180-010. Lot numbers 200515007, 200731007, 200924011, and 201001028 are affected.
Look for the catalog number 6770-180-010 and lot numbers listed above on the product label.
The product label incorrectly states a 54-month shelf life when the actual shelf life is 36 months.
Check the product label for the catalog number 6770-180-010 and lot numbers 200515007, 200731007, 200924011, or 201001028. If you have these, contact Stryker for guidance.
No, the hazard is a labeling error, not a safety issue. The risk is low as the product is not expected to cause injury.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0246-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0246-2024 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.
