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. 1,053 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
1,053 in last 12 months

Showing 15881–15900 of 49,990 recalls

Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: FREESTYLE LANCETS 28G 100CT Item Number:2975670 Recalled by Cardinal Health...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: ONETOUCH ULTRASOFT LANCETS 100 COUNT Item Number: 3007788 Recalled by...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: ONETOUCH DELICA LANCETS 33G 100 COUNT Item Number: 5541628 Recalled by...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Boston Scientific Corporation

Recalled Item: EXALT Controller - Product Usage: intended for use with a Recalled by Boston...

The Issue: May have been programmed with a less than optimal brightness setting...

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

Class III — Low RiskOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: ONETOUCH ULTRA TEST STRIPS 25 COUNT Item Number: 3510443 Recalled by...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Biomerieux Inc

Recalled Item: VIDAS¿ CMV IgM 30 Tests Recalled by Biomerieux Inc Due to bioMerieux...

The Issue: bioMerieux received complaints about calibration issue observed on several...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: BD UF PEN 32GX4MM 100 NANO Item Number: 4292272 Recalled by Cardinal Health...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: ONETOUCH DELICA LANCETS 30G 100 COUNT Item Number: 5541610 Recalled by...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Medtronic Inc.

Recalled Item: Medtronic Abre Venous Self-expanding Sent System Recalled by Medtronic Inc....

The Issue: Incorrect size printed on the device; packaging is labeled correctly.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: Oncology Kit w/60" (152 cm) Appx 2.2 ml Recalled by ICU Medical, Inc. Due to...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: 20mL Syringe w/Spinning Spiros Recalled by ICU Medical, Inc. Due to Due to...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: Admin Set w/ClaveTM Recalled by ICU Medical, Inc. Due to Due to molding...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx 3.2 ml Recalled by ICU Medical, Inc. Due to Due to molding...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: 5" (13 cm) Bag Spike Adapter w/Spiros" w/Red Cap Recalled by ICU Medical,...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: Spiros Closed Male Luer - Product Usage: provides Recalled by ICU Medical,...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: Oncology Kit w/Spiros¿ Recalled by ICU Medical, Inc. Due to Due to molding...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: 45" (114 cm) Appx 1.7 ml Recalled by ICU Medical, Inc. Due to Due to molding...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx 6.1 ml Recalled by ICU Medical, Inc. Due to Due to molding...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: 5" (13 cm) Appx 0.50 ml Recalled by ICU Medical, Inc. Due to Due to molding...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx 4.1 ml Recalled by ICU Medical, Inc. Due to Due to molding...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing