# FDA recall Z-1311-2025

> **Aesculap Inc** · Class II · device recall initiated 2025-01-31.

## Product

Numerous models of nonsterile hemostatic forceps:    (1) REF FB458R, Glover ATR.CLAMP CVD 215MM;  (2) REF FB459R, Glover ATR.CLAMP CVD 245MM;   (3) REF FB461R, Glover ATR.CLAMP 195MM;  (4) REF FB462R, Glover ATR.CLAMP 210MM;  (5) REF FB469R, Leland-Jones Peripheral CLMPSTR 195MM;  (6) REF FB567R, Cooley Pediatric Clamp 30DG30/165MM;  (7) REF FB568R, Cooley Pediatric Clamp 60DG 30/160MM;  (8) REF FB569R, Cooley Pediatric Clamp 90DG30/150MM;  (9) REF FB729R, Cooley Pediatric Clamp 17MM 170MM;  (10) REF FB730R, Cooley Pediatric Clamp 20MM175MM;  (11) REF FB736R, Cooley Pediatric Clamp 74MM 185MM;  (12) REF FB737R, Cooley Pediatric Clamp 86MM 195MM; and  (13) REF FB738R, Cooley Pediatric Clamp 108MM 260MM.

## Reason for recall

The forceps have been used in ways not covered by the design resulting in breakage of the clamps.

## Distribution

Distribution was made nationwide and to PR.  There was also government/military distribution.    Foreign distribution was made to Canada, Bermuda, Bahamas, and Qatar.

## Key facts

- **Recall number:** Z-1311-2025
- **Recalling firm:** Aesculap Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-01-31
- **Report date:** 2025-03-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Center Valley, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1311-2025

## Citation

> AI Analytics. FDA recall Z-1311-2025. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1311-2025. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*