UNIMAX Medical Systems recalls specific detachable endo retrieval pouches due to risk of tube falling into surgical site during grasping. Affected models include TM2001, TM2000, TM2002, FEP936116, FEP979000, SB936, SB957, SB979, SB979-CA, and SB936-CA with specific lot numbers.
The tube may fall into the surgical site during the grasping process.
UNIMAX Medical Systems recalls several detachable endo retrieval pouches that may fall into the surgical site during use, potentially causing complications. This recall affects specific model numbers and lot numbers used in medical procedures.
The pouch tube may fall into the surgical site during the grasping process, which could lead to complications such as bleeding or infection. This risk occurs when the pouch is being handled during surgical procedures.
Medical professionals using these pouches during surgery are most at risk. Patients undergoing procedures with the recalled pouches could face complications if the tube falls into the surgical site.
Check for model numbers: TM2001 (3" x 6"), TM2000 (5" x 7"), TM2002 (8" x 10"), FEP936116 (3" x 6"), FEP979000 (8" x 10"), SB936 (3" x 6"), SB957 (5" x 7"), SB979 (7.5" x 9"), SB979-CA (7.5" x 9"), and SB936-CA (3" x 6"). Also check lot numbers listed in the recall notice.
Identify the model number and lot numbers from the recall list to confirm if your pouch is affected.
The recall affects UNIMAX Medical Systems detachable endo retrieval pouches with model numbers TM2001, TM2000, TM2002, FEP936116, FEP979000, SB936, SB957, SB979, SB979-CA, and SB936-CA, each with specific lot numbers.
Check the model number and lot numbers listed in the recall notice. Affected models include TM2001 (3" x 6"), TM2000 (5" x 7"), TM2002 (8" x 10"), FEP936116 (3" x 6"), FEP979000 (8" x 10"), SB936 (3" x 6"), SB957 (5" x 7"), SB979 (7.5" x 9"), SB979-CA (7.5" x 9"), and SB936-CA (3" x 6").
Check the model number and lot numbers to confirm if your pouch is affected. If it is, contact UNIMAX Medical Systems for further instructions.
We’ve drafted a message you can send UNIMAX Medical Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-3164-2024 — UNIMAX Medical Systems UNIMAX Medical Systems Hello, I own a UNIMAX Medical Systems that is covered by recall Z-3164-2024 from UNIMAX Medical 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.
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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.
