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. 2,623 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,623 in last 12 months

Showing 86618680 of 28,355 recalls

Medical DeviceDecember 22, 2021· Empowered Diagnostics LLC

Recalled Item: ImmunoPass Recalled by Empowered Diagnostics LLC Due to COVID test kits were...

The Issue: COVID test kits were offered for sale and distributed to consumers in the...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2021· Empowered Diagnostics LLC

Recalled Item: CovClear COVID-19 Rapid Antigen Test Recalled by Empowered Diagnostics LLC...

The Issue: COVID test kits were offered for sale and distributed to consumers in the...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2021· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Philips has...

The Issue: Philips has identified a specific lot of non-conforming material...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2021· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Repair Kit Recalled by Philips Respironics, Inc. Due to Philips...

The Issue: Philips has identified a specific lot of non-conforming material...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 21, 2021· Medtronic Vascular, Inc.

Recalled Item: Endurant Recalled by Medtronic Vascular, Inc. Due to Stent Graft Systems...

The Issue: Stent Graft Systems built with specific batches of taper tip assemblies have...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2021· Vyaire Medical

Recalled Item: bellavista 1000 ventilator Recalled by Vyaire Medical Due to Potential...

The Issue: Potential cessation in ventilation can occur under specific conditions.

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 20, 2021· Canon Medical System, USA, INC.

Recalled Item: Flat Panel Detector Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Abnormal images such as horizontal stripes may be displayed and recovery may...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2021· Nobel Biocare Usa Llc

Recalled Item: NobelReplace Conical Connection RP 4.3x11.5 mm STERILE R Recalled by Nobel...

The Issue: Due to 16 complaints related to drivers not engaging in implants. According...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2021· Covidien Llc

Recalled Item: Chameleon PTA Balloon Dilation Catheter 8 mm x 40 mm Recalled by Covidien...

The Issue: The firm has received six (6) complaint reports from customers indicating...

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

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

Recalled Item: Draeger Fabius MRI Anesthesia Machine Recalled by Draeger Medical, Inc. Due...

The Issue: 26 Fabius MRI Anesthesia machines were distributed with internal hoses...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2021· CellEra LLC

Recalled Item: 20545 Vitale Silver calcium Alginate Dressings 4x5 Recalled by CellEra LLC...

The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...

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

Class III — Low RiskOngoing
Medical DeviceDecember 15, 2021· CellEra LLC

Recalled Item: 20522 Vitale Silver calcium Alginate Dressings 2x2 Recalled by CellEra LLC...

The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...

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

Class III — Low RiskOngoing
Medical DeviceDecember 15, 2021· CellEra LLC

Recalled Item: 20500 Vitale Silver calcium Alginate Dressing Ropes Recalled by CellEra LLC...

The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...

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

Class III — Low RiskOngoing
Medical DeviceDecember 15, 2021· CellEra LLC

Recalled Item: 20544 Vitale Silver calcium Alginate Dressings 4x4 Recalled by CellEra LLC...

The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...

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

Class III — Low RiskOngoing
Medical DeviceDecember 15, 2021· CellEra LLC

Recalled Item: 20548 Vitale Silver calcium Alginate Dressings 4x8 Recalled by CellEra LLC...

The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...

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

Class III — Low RiskOngoing
Medical DeviceDecember 14, 2021· Smith & Nephew, Inc.

Recalled Item: Acufex Access Advanced Positioning Kit - indicated for use to Recalled by...

The Issue: Products were shipped to the Global Distribution Center instead of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2021· Collagen Matrix, Inc.

Recalled Item: DuraMatrix-Onlay Collagen Dura Substitute Membrane 4 inches x 5 inches...

The Issue: Outer packaging (outer pouch) is not sealed compromising sterility and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2021· Collagen Matrix, Inc.

Recalled Item: RESODURA matrix onlay 10.0 cm x 12.5 cm - indicated Recalled by Collagen...

The Issue: Outer packaging (outer pouch) is not sealed compromising sterility and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2021· Olympus Corporation of the Americas

Recalled Item: OER-Elite Endoscope Reprocessor-for use in cleaning and high-level...

The Issue: The detergent and alcohol tank tubing may have been incorrectly assembled in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2021· FEMSelect Ltd

Recalled Item: The EnPlace is a single use trans-vaginal pelvic floor repair Recalled by...

The Issue: Certain lots may not have been packaged wth the Channel Tube Limiter.

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

Class II — Potential Health HazardOngoing