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. 1,995 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
1,995 in last 12 months

Showing 76417660 of 28,355 recalls

Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Cope Mandril Wire Guide (Stainless Steel) Recalled by Cook Incorporated Due...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Double Flexible Tipped Wire Guide Recalled by Cook Incorporated Due to Cook...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Fixed Core Wire Guide Recalled by Cook Incorporated Due to Cook Medical...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Amplatz extra Stiff Wire Guide Recalled by Cook Incorporated Due to Cook...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Rosen Curved Wire Guide Recalled by Cook Incorporated Due to Cook Medical...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Roadrunner PC Wire Guide (The Firm LT) Recalled by Cook Incorporated Due to...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Bentson Plus Wire Guide (Extra Body/20cm Distal Flexibility with Softened...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Newton Wire Guide (LT Taper/10cm Distal Flexibility) Recalled by Cook...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Vinyl Connecting Tube Recalled by Cook Incorporated Due to Cook Medical...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Heavy Double Flexible Tipped Wire Guide Recalled by Cook Incorporated Due to...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· Cook Incorporated

Recalled Item: Fixed Core Wire Guide (Safe-T-J Curved) Recalled by Cook Incorporated Due to...

The Issue: Cook Medical identified that devices from the affected device lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2022· Olympus Corporation of the Americas

Recalled Item: Olympus POWERSEAL 5MM Recalled by Olympus Corporation of the Americas Due to...

The Issue: An out of specification component preventing the blue retention ring from...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2022· Olympus Corporation of the Americas

Recalled Item: Olympus POWERSEAL 5MM Recalled by Olympus Corporation of the Americas Due to...

The Issue: An out of specification component preventing the blue retention ring from...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2022· Olympus Corporation of the Americas

Recalled Item: Olympus POWERSEAL 5MM Recalled by Olympus Corporation of the Americas Due to...

The Issue: An out of specification component preventing the blue retention ring from...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2022· SEDECAL SA

Recalled Item: Sedecal Soltus Battery Mobile X-Ray System 450 Battery Recalled by SEDECAL...

The Issue: Due to un-commanded movement of mobile x-ray unit.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2022· DeRoyal Industries Inc

Recalled Item: DeRoyal Sterile Custom Kits containing ICU Medical MicroClave Clear...

The Issue: Procedure packs contained a recalled product.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2022· Encore Medical, LP

Recalled Item: EMPOWER 3D Knee Tibial Insert Recalled by Encore Medical, LP Due to Hip...

The Issue: Hip liner implant boxes may contain knee inserts and knee insert boxes may...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2022· Encore Medical, LP

Recalled Item: EMPOWR Acetabular System Recalled by Encore Medical, LP Due to Hip liner...

The Issue: Hip liner implant boxes may contain knee inserts and knee insert boxes may...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2022· Exactech, Inc.

Recalled Item: GXL acetabular liners Recalled by Exactech, Inc. Due to Specific GXL...

The Issue: Specific GXL acetabular polyethylene liners, packaged in non-conforming...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2022· Exactech, Inc.

Recalled Item: GXL acetabular liners Recalled by Exactech, Inc. Due to Specific GXL...

The Issue: Specific GXL acetabular polyethylene liners, packaged in non-conforming...

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

Class II — Potential Health HazardOngoing