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. 2,661 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,661 in last 12 months

Showing 16211640 of 49,990 recalls

FoodAugust 14, 2025· Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Recalled Item: Frozen AquaStar Breaded Shrimp Recalled by Admiralty Island Fisheries Inc...

The Issue: Product may be contaminated with Cesium-137 (Cs-137).

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 14, 2025· Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Recalled Item: Frozen Mercado Kroger Cooked Shrimp - Medium - Peeled - Recalled by...

The Issue: Product may be contaminated with Cesium-137 (Cs-137).

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 14, 2025· Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Recalled Item: AquaStar Cocktail Shrimp Recalled by Admiralty Island Fisheries Inc dba...

The Issue: Product may be contaminated with Cesium-137 (Cs-137).

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 13, 2025· Penner Patient Care, Inc.

Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...

The Issue: The device does not bear a unique device identifier.

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2025· Penner Patient Care, Inc.

Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...

The Issue: The device does not bear a unique device identifier.

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2025· Penner Patient Care, Inc.

Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...

The Issue: The device does not bear a unique device identifier.

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2025· Penner Patient Care, Inc.

Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...

The Issue: The device does not bear a unique device identifier.

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2025· Penner Patient Care, Inc.

Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...

The Issue: The device does not bear a unique device identifier.

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2025· Penner Patient Care, Inc.

Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...

The Issue: The device does not bear a unique device identifier.

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2025· Penner Patient Care, Inc.

Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...

The Issue: The device does not bear a unique device identifier.

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2025· Penner Patient Care, Inc.

Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...

The Issue: The device does not bear a unique device identifier.

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2025· Penner Patient Care, Inc.

Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...

The Issue: The device does not bear a unique device identifier.

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2025· Penner Patient Care, Inc.

Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...

The Issue: The device does not bear a unique device identifier.

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2025· CHANGE HEALTHCARE CANADA COMPANY

Recalled Item: Change Healthcare Radiology Solutions software version 14.2.2 Recalled by...

The Issue: Due to software issue, radiology reports may not be fully displayed when...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. Brilliance iCT Recalled by...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. IQon Spectral CT Recalled by...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. Big Bore RT Recalled by...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. Ingenuity CT Family Brazil...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. CT 6000 Recalled by Philips...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. Brilliance 16 Power Recalled...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing