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 1288112900 of 28,355 recalls

Medical DeviceOctober 21, 2019· Cook Inc.

Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...

The Issue: The potential compromise of the sterility of products from an undersealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Cook Inc.

Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...

The Issue: The potential compromise of the sterility of products from an undersealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Cook Inc.

Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...

The Issue: The potential compromise of the sterility of products from an undersealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Cook Inc.

Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...

The Issue: The potential compromise of the sterility of products from an undersealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Cook Inc.

Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...

The Issue: The potential compromise of the sterility of products from an undersealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Cook Inc.

Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...

The Issue: The potential compromise of the sterility of products from an undersealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Cook Inc.

Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...

The Issue: The potential compromise of the sterility of products from an undersealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Cook Inc.

Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...

The Issue: The potential compromise of the sterility of products from an undersealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Cook Inc.

Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...

The Issue: The potential compromise of the sterility of products from an undersealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Cook Inc.

Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...

The Issue: The potential compromise of the sterility of products from an undersealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Cook Inc.

Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...

The Issue: The potential compromise of the sterility of products from an undersealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Cook Inc.

Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...

The Issue: The potential compromise of the sterility of products from an undersealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Cook Inc.

Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...

The Issue: The potential compromise of the sterility of products from an undersealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Cook Inc.

Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...

The Issue: The potential compromise of the sterility of products from an undersealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Cook Inc.

Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...

The Issue: The potential compromise of the sterility of products from an undersealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2019· Capso Vision, Inc.

Recalled Item: CapsoCAM Plus Recalled by Capso Vision, Inc. Due to Capsule Endoscopy...

The Issue: Capsule Endoscopy System: a defect present in the capsule window may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2019· Brasseler USA I Lp

Recalled Item: BRASSELER KM166-310-35 Twist Drill Quick Connect Diameter 3.5 mm Recalled by...

The Issue: One lot of 3.5 mm twist drills were incorrectly laser etched as 2.5 mm the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2019· Tornier, Inc

Recalled Item: Aequalis Ascend Flex Humeral Stem: Part Number UDI DWF601A 3700386944475...

The Issue: During shipping, it is possible for the Aequalis Ascend Flex humeral stem to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2019· Philips North America, LLC

Recalled Item: HeartStart XL+ Defibrillator/Monitor Recalled by Philips North America, LLC...

The Issue: The rotary therapy selector switch may fail, resulting in unexpected device...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2019· Cuattro LLC

Recalled Item: CuattroDR System Software Recalled by Cuattro LLC Due to There is a...

The Issue: There is a potential that an image from a previous patient study to show up...

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

Class II — Potential Health HazardOngoing