Stryker recalls disposable Spetzler-Malis bipolar forceps with incorrect 54-month expiration date label (should be 36 months). Affected units have specific catalog numbers and lot numbers.
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 label showing 54 months instead of the correct 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 when the actual shelf life is 36 months. Using expired medical devices could potentially lead to reduced effectiveness or safety issues during procedures, though this is not a direct hazard like fire or injury.
Medical professionals who own or use the recalled disposable Spetzler-Malis bipolar forceps with catalog number 6770-180-005. Patients using these forceps during procedures are at low risk if the product is used within its actual shelf life.
Check for the catalog number 6770-180-005 on the product label. Affected units include specific lot numbers: 200525007, 200806005, and 200910009.
Verify the expiration date on the product label matches the actual 36-month shelf life (not 54 months).
The product label incorrectly states a 54-month shelf life when the actual shelf life is 36 months.
Check the expiration date on the label; if it shows 54 months, it's affected. Contact Stryker for guidance.
This is a low-risk issue as the product may still be safe if used within its actual 36-month shelf life.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0245-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0245-2024 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.
