American Contract Systems recalls SPINE LUMBAR PACK models UTSL72AA/UTSL7: Possible treatment delays due to unconfirmed sterilization. Affected units sold with specific lot numbers.
ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
American Contract Systems is recalling SPINE LUMBAR PACK models UTSL72AA and UTSL72AB because they may not have been properly sterilized. This could cause delays or prolonged treatment for patients needing spinal surgery.
The products may not have been properly sterilized during manufacturing. This could lead to treatment delays or longer recovery times if the packs are used without proper sterilization.
Patients undergoing spinal surgery who use these specific models of SPINE LUMBAR PACKs are most at risk. Healthcare providers using these products in medical settings may also be affected.
Check for model numbers UTSL72AA or UTSL72AB on the product. Affected units include specific lot numbers: 939241, 88241, 70-052063, 70-052618A, and 70-053157.
Look for model numbers UTSL72AA or UTSL72AB on the SPINE LUMBAR PACK.
American Contract Systems cannot confirm that the products were properly sterilized, which may cause treatment delays or prolonged recovery.
The recall record does not specify a remedy, so no action is required beyond checking the model number.
Yes, affected units include lot numbers 939241, 88241, 70-052063, 70-052618A, and 70-053157.
We’ve drafted a message you can send American Contract Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-1360-2025 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-1360-2025 from American Contract Systems. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.