Stryker recalls disposable 5 lead cable and lead wire systems that may contain reprocessed ECG leads not approved for reuse, potentially causing device malfunction.
Disposable 5 lead cable and lead wire system package that should contain lead systems, lead telemetry systems and a dual connect cable, may in fact contain, different ECG Leads, which are not approved for reprocessing, but that may have been reprocessed, which may lead to devices not performing as intended.
Stryker is recalling disposable 5 lead cable and lead wire systems that may contain reprocessed ECG leads not approved for reprocessing. This could cause medical devices to not function properly during use.
The recalled cable packages may contain ECG leads that have been reprocessed but are not approved for reuse. This could lead to medical devices not performing as intended during patient monitoring.
Medical professionals using these specific cable systems for ECG monitoring are most at risk if they use the recalled items. Patients receiving care with these systems could experience improper device function.
Check for the model reference LW-309DS50/5A on the packaging. The lot numbers listed in the recall include specific sequences like 0000111423 through 13325718.
Verify the model reference LW-309DS50/5A and lot numbers listed in the recall to confirm if your item is affected.
The recall is because the cable packages may contain ECG leads that have been reprocessed but are not approved for reuse, which could cause medical devices to not function properly.
The official recall notice does not specify a remedy or action to take for affected products.
The recall indicates a potential risk of medical devices not functioning properly, but the official notice does not describe a risk of injury or serious harm.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2689-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2689-2024 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.
