FDA recall record

UNIMAX MEDICAL SYSTEMS 1. Tech Medical Services Inc. Detachable Endo Retrieval Pouch, REF recall — FDA Z-3164-2024

The tube may fall into the surgical site during the grasping process.

Class IIclassification
Z-3164-2024official record ID
Sep 25, 2024report date

Recall record at a glance

Official recordZ-3164-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmUNIMAX MEDICAL SYSTEMS Inc.
Report dateSep 25, 2024
Recall initiation dateJun 25, 2024
Quantity81,241 endo retrieval pouches
LocationHsin Tien, Taiwan

Official product description

1. Tech Medical Services Inc. Detachable Endo Retrieval Pouch, REF TM2001, 3" x 6", sterile; 2. Tech Medical Services Inc. Detachable Endo Retrieval Pouch, REF TM2000, 5" x 7", sterile; 3. Tech Medical Services, Inc. Detachable Endo Retrieval Pouch, REF TM2002, 8" x 10", sterile; 4. UNIMAX Detachable endo pocket, REF FEP936116, 3" x 6", sterile; 5. UNIMAX Detachable endo pocket, REF FEP979000, 8" x 10", sterile; 6. ConMed Corporation Detachable endo pocket, REF SB936, 3" x 6", sterile; 7. ConMed Corporation Detachable endo pocket, REF SB957, 5" x 7", sterile; 8. ConMed Corporation Detachable endo pocket, REF SB979, 7.5" x 9", sterile; 9. ConMed Corporation Detachable endo pocket, REF SB979-CA, 7.5 x 9", sterile; 10. ConMed Corporation Detachable endo pocket, REF SB936-CA, 3" x 6", sterile;

Why the product was recalled

The tube may fall into the surgical site during the grasping process.

Distribution information

US Nationwide distribution in the states of GA, MO, and PA.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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