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American Contract Systems Inc

American Contract Systems Inc Recalls

All product recalls associated with American Contract Systems Inc.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

145

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1941–1960 of 37661 recalls

Delivery Pack (American Contract) – sterilization uncertainty (2025)

ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.

Moderate

FDAFeb 6, 2025Nationwide• American Contract Systems Inc

RYOBI 40-Volt Mowers (TTI) – Fire Hazard (2025)

Fire/Burn Risk

This recall involves certain RYOBI Brushless 21" Cordless Walk-Behind Self-Propelled Multi-Blade Push Mowers (40V HP). The mowers have a black cutting deck with gray top housing along with a black bag with "RYOBI" printed on it. The recall only includes model numbers RY401014BTLUS, RY401014US, RY401140US, RY401015BTLUS, RY401015US, RY401150US, RY401140US-Y, RY401150US-Y, RY401020, and RY401200 with the following serial numbers: KC21032D010001 - KC21327N999999. The model and serial numbers can be found on the mowers inside the green mower housing.

High

CPSCFeb 6, 2025Nationwide• TTI Outdoor Power Equipment Inc., of Anderson, South Carolina

1...96 979899 100...1884

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Morphine Sulfate Tablets (Sun Pharma) – Dissolution Failure (2025)

Failed Dissolution Specifications

Class IIModerate

FDAFeb 6, 2025Nationwide• SUN PHARMACEUTICAL INDUSTRIES INC

Alfalfa Sprouts (Jack & Green Sprouts) – Listeria Contamination (2025)

Listeria

Sprouts have the potential to be contaminated with Listeria monocytogenes

Class IHigh

FDAFeb 6, 2025IA, MN, WI• Jack & The Green Sprouts, Inc.

Laparoscopy Pack (American Contract) – sterilization uncertainty (2025)

ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.

Moderate

FDAFeb 6, 2025Nationwide• American Contract Systems Inc

Laceration Tray (American Contract) – sterilization uncertainty (2025)

ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.

Moderate

FDAFeb 6, 2025Nationwide• American Contract Systems Inc

DxI 9000 Analyzer (Beckman Coulter) – interface board issue (2025)

Beckman Coulter identified that an issue for DxI 9000 tip stocker interface (TSI) and reagent storage interface (RSI) boards with the firmware version 1.1.0.0 can cause sub-system communication failures. This failure could result in a delay in reporting patient results.

Moderate

FDAFeb 6, 2025Nationwide• Beckman Coulter, Inc.

Rotarex Atherectomy System (Bard) – catheter breakage (2025)

Atherectomy Catheter eIFU updated to clarify and emphasize procedural steps intended to reduce the likelihood of catheter breakage events. Catheter has an outer cylinder connected to a rotating helix, which could fracture and/or break, which would require retrieval, and helix facture/break could cause vessel injury and lead to severe bleeding.

High

FDAFeb 5, 2025Nationwide• Bard Peripheral Vascular Inc 1625 W 3rd St Bldg 1 850 W. Rio Salado Prkwy. Tempe AZ 85281-2438

DxI 9000 Analyzer (Beckman Coulter) – encoder wheel misalignment (2025)

the DxI 9000 encoder wheel was misaligned on the motor shaft, leading to increased slippage errors and causing the instrument to stop, posing a high safety risk due to potential delays in patient results.

Moderate

FDAFeb 5, 2025Nationwide• Beckman Coulter, Inc.

Spectrum IQ Infusion System (Baxter) – mounting screw issue (2025)

There is the potential for missing motor mounting screws, which may have occurred during the servicing process.

Moderate

FDAFeb 5, 2025Nationwide• Baxter Healthcare Corporation

MEDITECH Expanse Software (Medical Information Technology) – data removal (2025)

Entering multiple keys that trigger input simultaneously may remove data from first field of screens and/or questionnaires with more than one field.

Low

FDAFeb 5, 2025Nationwide• Medical Information Technology, Inc.

Sigma Spectrum Infusion System (Baxter) – mounting screw issue (2025)

There is the potential for missing motor mounting screws, which may have occurred during the servicing process.

Moderate

FDAFeb 5, 2025Nationwide• Baxter Healthcare Corporation

Aortic Root Cannula (Medtronic) – luer material issue (2025)

Unexpected loose material in the male luer used in the aortic root cannula has been identified. Potential harms when identified prior to use - procedure delay. Potential harm if not identified and used - stroke (reversible and irreversible).

High

FDAFeb 5, 2025Nationwide• Medtronic Perfusion Systems

Access 2 Analyzer (Beckman Coulter) – sample motor alignment (2025)

Beckman Coulter identified that an issue for Access 2 Sample Motors (B48016) due to improper alignment, causing the motors to rub against the sample wheelbase plate and index sensor. The issue was traced to a worn tool used in production (at the supplier), affecting Access 2 sample motors. This could lead to a potential delay in reporting patient test results.

Moderate

FDAFeb 5, 2025Nationwide• Beckman Coulter, Inc.

IntelePACS Software (Intelerad) – image calculation error (2025)

A software application that receives digital images and data from various sources has a bug in specific software versions that will calculate the Standard Uptake Value (SUV) incorrectly for PET/CT studies acquired on the days of Daylight Savings Time (DST); only on dates in which DST transition occurs; all other dates are unaffected. An incorrect SUV may lead to an incorrect diagnosis.

High

FDAFeb 5, 2025Nationwide• INTELERAD MEDICAL SYSTEMS INCORPORATED 800, Boul. de Maisonneuve Est 12th floor Montreal Canada

Organic Acai Bowl (Stiebs) – Plastic Contamination (2025)

Potential contamination with blue pieces of plastic

Class IIModerate

FDAFeb 5, 2025CA, CT, IL +3 more• Stiebs, LLC

Crani Pack (American Contract) – sterilization uncertainty (2025)

During an internal investigation, ACS was unable to confirm that the CODMAN component achieved the required Sterility Assurance Level and therefore is not suitable for sterilization according to ACS procedures.

Moderate

FDAFeb 4, 2025MI• American Contract Systems Inc