American Contract Systems Inc.: Device Recall

Recall #Z-0171-2026 · 09/04/2025

Class II: Risk

Recall Details

Recall Number
Z-0171-2026
Classification
Class II
Product Type
Device
Recalling Firm
American Contract Systems Inc.
Status
Ongoing
Date Initiated
09/04/2025
Location
Grimes, IA, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
32,433 total

Reason for Recall

Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process. These products have not been validated for exposure to multiple sterilization cycles. Therefore, product quality, safety, and effectiveness cannot be confirmed for product that was re-gassed.

Product Description

Basic Biopsy Tray; Item Number/Description: AKRB26D ROBOTIC, AMGL09AA GENERAL LAPAROSCOPY, ANLC35AD LAP CHOLE PACK - 205956, ANLP25AJ LAPROSCOPY PACK - 205958, FYLA38E LAPCHOLAPPY PACK, IHDA88AH DIVINCI GYN URO, IHLC11AE LAP GENERAL PACK, MHLP45AJ LAPAROSCOPY PACK - 206005, MHRB88AO ROBOTIC PACK - 242561, RCLC51C LAP CHOLE RCH 0246969, SMLC53C LAP CHOLE PACK, UDLC17AE DSC LAP CHOLE PACK - 206062, UIRU84AE ROBOTIC UROLOGY PACK (PS 060571)

Distribution Pattern

US Nationwide distribution in the states of SD, IA, MN, WA, IL.

Other Recalls by American Contract Systems Inc.

View all recalls by American Contract Systems Inc. →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.