Stryker recalls expired bone cement delivery needles (catalog 1025-011-500) that may pose safety risks. Affected products were distributed to customers with specific lot numbers.
Expired Products distributed to customers
Stryker is recalling bone cement delivery needles that have expired. These needles are used in spinal procedures to inject bone cement. If you own an expired needle, stop using it immediately to avoid potential safety risks.
Expired products can lose effectiveness and safety over time. Using expired medical devices may lead to improper procedures or complications during spinal injections.
Physicians who use these needles for spinal procedures may be affected. Patients receiving the procedure are at risk if the expired product is used.
Check for catalog number 1025-011-500 and lot number 6659783 on the needle packaging. These products were distributed to customers starting from the date of manufacture.
Look for catalog number 1025-011-500 and lot number 6659783 on the needle packaging.
The recall is for expired products distributed to customers, which may pose safety risks.
The official notice does not specify a remedy for expired products.
Check for catalog number 1025-011-500 and lot number 6659783 on the packaging.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2260-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2260-2024 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.
