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 1206112080 of 28,355 recalls

Medical DeviceMarch 17, 2020· Radiometer Medical ApS

Recalled Item: safeCLINITUBES Blood Sampler Recalled by Radiometer Medical ApS Due to The...

The Issue: The SafeCLINITUBES blood sampler may have insufficient aspiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Radiometer Medical ApS

Recalled Item: safeCLINITUBES Blood Sampler Recalled by Radiometer Medical ApS Due to The...

The Issue: The SafeCLINITUBES blood sampler may have insufficient aspiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Radiometer Medical ApS

Recalled Item: safeCLINITUBES Blood Sampler Recalled by Radiometer Medical ApS Due to The...

The Issue: The SafeCLINITUBES blood sampler may have insufficient aspiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Applied Medical Resources Corp

Recalled Item: DR. THAMES - LAP CHOLE Recalled by Applied Medical Resources Corp Due to...

The Issue: There may be a slightly protruding rivet on the distal end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Applied Medical Resources Corp

Recalled Item: Clip Applier Kit Recalled by Applied Medical Resources Corp Due to There may...

The Issue: There may be a slightly protruding rivet on the distal end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Applied Medical Resources Corp

Recalled Item: Epix latis GRASPER Recalled by Applied Medical Resources Corp Due to There...

The Issue: There may be a slightly protruding rivet on the distal end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Applied Medical Resources Corp

Recalled Item: Epix latis GRASPER Recalled by Applied Medical Resources Corp Due to There...

The Issue: There may be a slightly protruding rivet on the distal end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew FOOTPRINT Ultra PK Suture Anchor Recalled by Smith & Nephew,...

The Issue: Space between the device and the packaging permits excessive movement which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Rayner Intraocular Lenses Limited

Recalled Item: RaySert PLUS RSP01. LOT K030. Expiry of 2024-01 - Product Recalled by Rayner...

The Issue: RaySert PLUS RSP01 LOT K030 labeled with an expiry of 2024-01 contained an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing