# FDA recall Z-3164-2024

> **UNIMAX MEDICAL SYSTEMS INC** · Class II · device recall initiated 2024-06-25.

## Product

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;

## Reason for recall

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

## Distribution

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

## Key facts

- **Recall number:** Z-3164-2024
- **Recalling firm:** UNIMAX MEDICAL SYSTEMS INC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-06-25
- **Report date:** 2024-09-25

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Hsin Tien, Taiwan

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3164-2024

## Citation

> AI Analytics. FDA recall Z-3164-2024. Retrieved 2026-07-02 from https://api.ai-analytics.org/recall/Z-3164-2024. Source: US FDA. Licensed CC0.

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