# FDA recall Z-2655-2026

> **Bard Access Systems, Inc.** · Class II · device recall initiated 2026-05-21.

## Product

OTP5000	THORA/PARA TRAY, 5FR, NON-VALVED  UDI-DI Code: 0110885403284748    PIG1260T	SAFE-T-CENTESIS TRAY 6FR X 16CM  UDI-DI Code: 0110885403108365    TPT1000	THORACENTESIS/PARACENTESIS TRAY  UDI-DI Code: 0110885403108488      The Acute Drainage devices are indicated for use in removing fluid from either the pleural or peritoneal spaces during an acute drainage / aspiration procedure.

## Reason for recall

Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

## Distribution

Worldwide U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, and WY. The country of Belgium.

## Key facts

- **Recall number:** Z-2655-2026
- **Recalling firm:** Bard Access Systems, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-05-21
- **Report date:** 2026-07-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Salt Lake City, UT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2655-2026

## Citation

> MORVS. FDA recall Z-2655-2026. Retrieved 2026-10-21 from https://api.morvs.ai/recall/Z-2655-2026. Source: US FDA. Licensed CC0.

---

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