Product Recalls in Washington

Product recalls affecting Washington — including food, drugs, consumer products, medical devices, and vehicles distributed to Washington. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,183 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
1,183 in last 12 months

Showing 1661–1680 of 51,768 recalls

Medical DeviceAugust 15, 2025· Maquet Cardiovascular, LLC

Recalled Item: Heartstring III Proximal Seal System. Intravascular anastomosis occluder....

The Issue: Three failure modes have been identified: failure of the Heartstring Seal to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2025· ETHICON, LLC

Recalled Item: STRATAFIX Spiral PDS Plus Bidirectional Knotless Tissue Control Device...

The Issue: Potential for barb non-engagement.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2025· Exactech, Inc.

Recalled Item: Exactech Equinoxe Recalled by Exactech, Inc. Due to Reverse Shoulder humeral...

The Issue: Reverse Shoulder humeral liners have an articular surface position outside...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2025· Maquet Cardiovascular, LLC

Recalled Item: Heartstring III Proximal Seal System Recalled by Maquet Cardiovascular, LLC...

The Issue: Three failure modes have been identified: failure of the Heartstring Seal to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2025· Maquet Cardiovascular, LLC

Recalled Item: Heartstring III Proximal Seal System Recalled by Maquet Cardiovascular, LLC...

The Issue: Three failure modes have been identified: failure of the Heartstring Seal to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2025· Exactech, Inc.

Recalled Item: Exactech Equinoxe Recalled by Exactech, Inc. Due to Reverse Shoulder humeral...

The Issue: Reverse Shoulder humeral liners have an articular surface position outside...

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

Class II — Potential Health HazardOngoing
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
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
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· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. Brilliance CT 40 Channel...

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
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. 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. 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. 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· Beckman Coulter Inc.

Recalled Item: UniCel DxH 800 COULTER Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Hematology analyzers configured with HGB photometers may result in...

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

Class II — Potential Health HazardOngoing