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. 2,765 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,765 in last 12 months

Showing 1554115560 of 51,768 recalls

Medical DeviceAugust 5, 2021· Beckman Coulter Inc.

Recalled Item: Access SARS CoV-2 IgG (1st IS) Assay: Access Immunoassay Systems REAGENT...

The Issue: Firm's submission for Emergency Use Authorization (EUA) contained...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2021· C.R. Bard Inc

Recalled Item: Catalog A399400A Recalled by C.R. Bard Inc Due to There is potential for...

The Issue: There is potential for packaging defects that may impact the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2021· C.R. Bard Inc

Recalled Item: Catalog A300316A Recalled by C.R. Bard Inc Due to There is potential for...

The Issue: There is potential for packaging defects that may impact the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2021· C.R. Bard Inc

Recalled Item: Catalog A902416 Recalled by C.R. Bard Inc Due to There is potential for...

The Issue: There is potential for packaging defects that may impact the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2021· Armstrong Medical Services Limited

Recalled Item: AMSORB PLUS PREFILLED G-CAN 1.0L Recalled by Armstrong Medical Services...

The Issue: Some devices may be associated with high and unexpected resistance to gas...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2021· Abbott Molecular, Inc.

Recalled Item: Vysis CLL FISH Probe Kit with the following components: Vysis Recalled by...

The Issue: Potential for Vysis CLL FISH Probe Kits not detecting 13q deletions in known...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2021· Roche Molecular Systems, Inc.

Recalled Item: cobas SARS-CoV-2 & Influenza A/B Test for use on the cobas Liat System...

The Issue: Customers have reported an increased number of false positive SARS-CoV-2...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2021· Mac Medical Supply Co Inc

Recalled Item: Ultrasound Gel labeled under the following brand names: MediChoice...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2021· Cardinal Health

Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Cardinal Health Due...

The Issue: Potential for the plunger to draw back after the air has been expelled and...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2021· Cardinal Health

Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Cardinal Health Due...

The Issue: Potential for the plunger to draw back after the air has been expelled and...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2021· Cardinal Health

Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Cardinal Health Due...

The Issue: Potential for the plunger to draw back after the air has been expelled and...

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

Class I — Serious Health HazardOngoing
DrugAugust 3, 2021· The Harvard Drug Group

Recalled Item: Fexofenadine Hydrochloride Tablets Recalled by The Harvard Drug Group Due to...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 3, 2021· Teligent Pharma, Inc.

Recalled Item: Lidocaine Hydrochloride Topical Solution Recalled by Teligent Pharma, Inc....

The Issue: Superpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 3, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: AquaBplus Water Purification System Recalled by Fresenius Medical Care...

The Issue: AquaBplus HF module on the AquaBplus 2000 osmosis system, an error in the US...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2021· Luminex Corporation

Recalled Item: Verigene EP Amplification Reagent Kit Test Recalled by Luminex Corporation...

The Issue: There is potential for false positive results.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2021· Olympus Corporation of the Americas

Recalled Item: Arc Endocuff Vision as follows: ARV110 ENDOCUFF-V M BLUE PK8 Recalled by...

The Issue: Packaging seal defect may allow a breach of the package sterile barrier and...

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

Class II — Potential Health HazardOngoing
DrugAugust 2, 2021· Je Dois Lavoir LLC

Recalled Item: 365 SKINNY High Intensity Capsules Recalled by Je Dois Lavoir LLC Due to...

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found the product to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 2, 2021· Akorn, Inc.

Recalled Item: Artificial Tears Ointment Recalled by Akorn, Inc. Due to Non-Sterility - OOS...

The Issue: Non-Sterility - OOS sterility testing observed during 12-month controlled...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2021· Macleods Pharma Usa Inc

Recalled Item: Clopidogrel Tablets Recalled by Macleods Pharma Usa Inc Due to Presence of...

The Issue: Presence of foreign matter

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 2, 2021· Golden Natural Products

Recalled Item: Golden Natural Product Inc. brand Dried Apricot Subkhon with Bone Recalled...

The Issue: Product contains high levels of undeclared sulfites.

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

Class I — Serious Health HazardOngoing
Refund