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 1506115080 of 49,990 recalls

FoodJune 21, 2021· Bea Lydeckers Naturals Inc

Recalled Item: Living Free Nerve & Muscle Herbal Dietary Supplement Recalled by Bea...

The Issue: Label declares lecithin but does not declare soy lecithin.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJune 21, 2021· Bea Lydeckers Naturals Inc

Recalled Item: Living Free "Adult Extra" multi-vitamin Recalled by Bea Lydeckers Naturals...

The Issue: Label declares lecithin but does not declare soy lecithin.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJune 21, 2021· Bea Lydeckers Naturals Inc

Recalled Item: Living Free Lung & Joint Congestion Herbal Dietary Supplement Recalled by...

The Issue: Label declares lecithin but does not declare soy lecithin.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJune 21, 2021· Bea Lydeckers Naturals Inc

Recalled Item: Living Free Heart/Blood Vessel Dietary Supplement Recalled by Bea Lydeckers...

The Issue: Label declares lecithin but does not declare soy lecithin.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 21, 2021· Murata Vios, Inc.

Recalled Item: muRata Vios Monitoring System Model 2050 Recalled by Murata Vios, Inc. Due...

The Issue: During the set-up and workflow to begin Vios monitoring, it has been noticed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Accora Inc

Recalled Item: Configura Advance Chair Recalled by Accora Inc Due to The firm has...

The Issue: The firm has identified a potential for the backrest to become detached from...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: NEO DELTA Self Safe Recalled by Delta Med SpA Due to Problems related to the...

The Issue: Problems related to the sterilization of the medical devices; possible...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: NEO DELTA Self Safe 1 Recalled by Delta Med SpA Due to Problems related to...

The Issue: Problems related to the sterilization of the medical devices; possible...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: NEO DELTA SELFSAFE PUR T Recalled by Delta Med SpA Due to Problems related...

The Issue: Problems related to the sterilization of the medical devices; possible...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: NEO DELTA Self Safe T Recalled by Delta Med SpA Due to Problems related to...

The Issue: Problems related to the sterilization of the medical devices; possible...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: DELTAVEN Y DNL Safety I.V. Catheter in Pur with closed Recalled by Delta Med...

The Issue: Problems related to the sterilization of the medical devices; possible...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: NEO DELTA SELFSAFE PUR T Recalled by Delta Med SpA Due to Problems related...

The Issue: Problems related to the sterilization of the medical devices; possible...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: WOLF-PAK Self Safe Safety IV Catheter: a) b) Recalled by Delta Med SpA Due...

The Issue: Problems related to the sterilization of the medical devices; possible...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: DELTAVEN Safety I.V. Catheter in Pur with closed system: a) Recalled by...

The Issue: Problems related to the sterilization of the medical devices; possible...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: DELTAVEN FASTFLASH Recalled by Delta Med SpA Due to Problems related to the...

The Issue: Problems related to the sterilization of the medical devices; possible...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: NEO DELTA SELFSAFE PUR 1 Recalled by Delta Med SpA Due to Problems related...

The Issue: Problems related to the sterilization of the medical devices; possible...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2021· Delta Med SpA

Recalled Item: DELTAVEN Y Recalled by Delta Med SpA Due to Problems related to the...

The Issue: Problems related to the sterilization of the medical devices; possible...

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

Class II — Potential Health HazardOngoing
DrugJune 18, 2021· Teva Pharmaceuticals USA

Recalled Item: Topotecan Injection 4 mg/4mL (1 mg/mL) Recalled by Teva Pharmaceuticals USA...

The Issue: Presence of Particulate Matter: Complaint received of a glass particle...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
FoodJune 18, 2021· Cuisine Solutions

Recalled Item: JUST Egg Inspired by Japan Portobello Recalled by Cuisine Solutions Due to...

The Issue: Undeclared egg and milk

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJune 18, 2021· Cuisine Solutions

Recalled Item: JUST Egg Inspired by America Roasted Potato Recalled by Cuisine Solutions...

The Issue: Undeclared egg and milk

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund