Product Recalls in Arkansas

Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,591 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,591 in last 12 months

Showing 1554115560 of 49,990 recalls

Medical DeviceApril 16, 2021· Draeger Medical, Inc.

Recalled Item: Critical Care Ventilator Recalled by Draeger Medical, Inc. Due to Three...

The Issue: Three separate and unrelated problems attributed to the software used in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2021· Draeger Medical, Inc.

Recalled Item: Critical Care Ventilator Recalled by Draeger Medical, Inc. Due to Three...

The Issue: Three separate and unrelated problems attributed to the software used in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2021· Draeger Medical, Inc.

Recalled Item: Critical Care Ventilator Recalled by Draeger Medical, Inc. Due to Three...

The Issue: Three separate and unrelated problems attributed to the software used in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2021· Draeger Medical, Inc.

Recalled Item: Critical Care Ventilator Recalled by Draeger Medical, Inc. Due to Three...

The Issue: Three separate and unrelated problems attributed to the software used in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugApril 15, 2021· Grace Healthcare Medical, Inc

Recalled Item: Oxygen Recalled by Grace Healthcare Medical, Inc Due to cGMP deviations

The Issue: cGMP deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 15, 2021· Vygon U.S.A.

Recalled Item: Vygon Dressing Change w/ Maxiswab - Product Usage: Custom Dressing Change...

The Issue: Compromised sterile barriers due to the Tyvek Lid not properly adhering to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2021· Flower Orthopedics Corporation

Recalled Item: T25 Cannulated Screwdrivers (CSD 025) packaged in Guide Wire Kits Recalled...

The Issue: Cannulated Screwdrivers may break at the driver tip along the shaft, near...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2021· Haag-Streit USA Inc

Recalled Item: Eyesuite 9.3.1 software Recalled by Haag-Streit USA Inc Due to Examination...

The Issue: Examination data and patient name may be mixed up when printing or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2021· Boston Scientific Corporation

Recalled Item: UpsylonTM Y Mesh Kit with Colpassist Vaginal Positioning Device - Recalled...

The Issue: Potential for pinholes (sterile barrier breach) on the edge of the pouch to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2021· Boston Scientific Corporation

Recalled Item: Colpassist Vaginal Positioning Device - Product Usage: intended for use...

The Issue: Potential for pinholes (sterile barrier breach) on the edge of the pouch to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugApril 14, 2021· Fresenius Medical Care, North America

Recalled Item: Delflex Peritoneal Dialysis Solution with 1.5% Dextrose Recalled by...

The Issue: Labeling; Label Mix-up; 4.25% DEXTROSE bag was found inside a 1.5% DEXTROSE box.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodApril 14, 2021· Reser's Fine Foods, Inc.

Recalled Item: Freshness Guaranteed Macaroni Salad Amish Recalled by Reser's Fine Foods,...

The Issue: Undeclared Wheat and/or Egg. The bottom label of Macaroni Salad Amish was...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 14, 2021· Dutch Ophthalmic USA, Inc.

Recalled Item: Illuminated Stepped Laser Probe Curved-for use in combination with 23G...

The Issue: Barcode label extended expiration date. Barcode located at the short side of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2021· Radiometer Medical ApS

Recalled Item: E3800 PC Units (spare parts) Recalled by Radiometer Medical ApS Due to Due...

The Issue: Due to an issue with the internal clock of the analyzers with an e3800 PC...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2021· Radiometer Medical ApS

Recalled Item: Radiometer ABL90 FLEX Analyzer with E3800 PC units. The E3800 Recalled by...

The Issue: Due to an issue with the internal clock of the analyzers with an e3800 PC...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2021· Radiometer Medical ApS

Recalled Item: Radiometer ABL90 FLEX PLUS Analyzer with E3800 PC units. The Recalled by...

The Issue: Due to an issue with the internal clock of the analyzers with an e3800 PC...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2021· Beckman Coulter Inc.

Recalled Item: Access SARS-CoV-2 Antigen Recalled by Beckman Coulter Inc. Due to specimens...

The Issue: specimens collected in transport media may result is false negative results...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugApril 13, 2021· Nomax Inc

Recalled Item: Dry Eye Test Recalled by Nomax Inc Due to Subpotent Drug

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodApril 13, 2021· Snak King Corporation

Recalled Item: Trader Joe's Restaurant Style White Corn Tortilla Chips Recalled by Snak...

The Issue: White Corn Tortilla Chips may contain undeclared milk

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 13, 2021· Philips North America Llc

Recalled Item: BRILLIANCE VOLUME system - A Computed Tomography X-Ray System intended...

The Issue: Cooling Unit (CLU) expelled out of a CT gantry of an iCT system may result...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing