Stryker Spine recalls LITe Decompression Snake Arm (REF 48080230) due to incorrect clamp component preventing attachment to arm post shaft. Affected units have UDI-DI GTIN 07613327263909, lot #227764.
Product arm was manufactured with the incorrect clamp component. As a result, the affected product arm cannot attach to the arm post shaft.
Stryker Spine is recalling LITe Decompression Snake Arms with the incorrect clamp component that prevents attachment to the arm post shaft. This could cause the device to malfunction during use, potentially leading to improper spinal decompression.
The product arm was manufactured with the wrong clamp component, so it cannot securely attach to the arm post shaft. This may cause the device to malfunction during spinal decompression procedures, potentially leading to improper treatment.
Medical professionals using the LITe Decompression Snake Arm for spinal procedures are most at risk. Patients using the device may also be affected if the arm fails to attach properly.
Check for the product name 'LITe Decompression Snake Arm' with reference number 48080230. Affected units have UDI-DI GTIN 07613327263909 and lot number 227764.
Verify the product name, reference number, and UDI-DI GTIN to confirm if your device is affected.
The LITe Decompression Snake Arm was manufactured with the incorrect clamp component, which prevents it from attaching to the arm post shaft.
Check for the product name 'LITe Decompression Snake Arm' with reference number 48080230. Affected units have UDI-DI GTIN 07613327263909 and lot number 227764.
The recall record does not specify a remedy, so contact Stryker Spine directly for guidance.
We’ve drafted a message you can send Stryker Spine to request your refund or repair — edit it as you like.
Subject: Recall Z-0610-2024 — Stryker Spine Stryker Spine Hello, I own a Stryker Spine that is covered by recall Z-0610-2024 from Stryker Spine. 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.
