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. 2,653 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,653 in last 12 months

Showing 2324123260 of 51,768 recalls

FoodApril 26, 2019· Oregons Wild Harvest Inc

Recalled Item: Dried whole elderberry Recalled by Oregons Wild Harvest Inc Due to Dried...

The Issue: Dried whole Elderberries are recalled due to glass fragments contamination.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 26, 2019· Inovo, Inc

Recalled Item: Inovo Single Luman Conserver Product Usage: This device is intended Recalled...

The Issue: The pressure gauge (manometer) may dislodge from the threaded...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2019· Cytocell Ltd.

Recalled Item: Aquarius D13S319 Plus Deletion Probe Recalled by Cytocell Ltd. Due to There...

The Issue: There is an error in the chromomap on the package insert.

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

Class III — Low RiskOngoing
Medical DeviceApril 26, 2019· PF Consumer Healthcare 1 LLC

Recalled Item: ThermaCare HEATWRAPS Recalled by PF Consumer Healthcare 1 LLC Due to There...

The Issue: There is the potential that a HeatWrap could include cells that have a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2019· Terumo Medical Corporation

Recalled Item: SOLOPATH Balloon Expandable TransFemoral System Recalled by Terumo Medical...

The Issue: There is a potential for dislodgement of the tip from the outer diameter of...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 26, 2019· Terumo Medical Corporation

Recalled Item: Portico Solo Re-Collapsible Access System Recalled by Terumo Medical...

The Issue: There is a potential for dislodgement of the tip from the outer diameter of...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 26, 2019· Terumo Medical Corporation

Recalled Item: SOLOPATH Re-Collapsible Access System Recalled by Terumo Medical Corporation...

The Issue: There is a potential for dislodgement of the tip from the outer diameter of...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 26, 2019· PF Consumer Healthcare 1 LLC

Recalled Item: ThermaCare HEATWRAPS Recalled by PF Consumer Healthcare 1 LLC Due to There...

The Issue: There is the potential that a HeatWrap could include cells that have a...

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

Class II — Potential Health HazardOngoing
DrugApril 25, 2019· Zydus Pharmaceuticals USA Inc

Recalled Item: Acyclovir Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to Labeling;...

The Issue: Labeling; Label Mix-up; report received of one bottle labeled as Acyclovir...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 25, 2019· Zydus Pharmaceuticals USA Inc

Recalled Item: Carvedilol Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to...

The Issue: Labeling; Label Mix-up; report received of one bottle labeled as Acyclovir...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 25, 2019· Advantice Health

Recalled Item: Dermoplast Anesthetic PAIN & ITCH (benzocaine and menthol) SPRAY canisters...

The Issue: Labeling: Not Elsewhere Classified: canisters incorrectly state the net...

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

Class III — Low RiskOngoing
Refund
DrugApril 25, 2019· Advantice Health

Recalled Item: Dermoplast Anesthetic PAIN & ITCH (benzocaine and menthol) SPRAY canisters...

The Issue: Labeling: Not Elsewhere Classified: Full cases may contain canisters that...

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

Class III — Low RiskOngoing
Refund
DrugApril 25, 2019· US Worldmeds LLC

Recalled Item: Revonto (dantrolene sodium for injection) Recalled by US Worldmeds LLC Due...

The Issue: Presence of Precipitate: Appearance is Out of Specification for the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 25, 2019· ASTRA, LLC

Recalled Item: Lidar System for Erosion Flume Application Class 1 Laser Product Recalled by...

The Issue: Failure to comply event due to incorrect labeling of a class 1 laser product.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2019· Medline Industries Inc

Recalled Item: Endoscopic Cleaning Brushes sold in various Endoscopy Kits - Product...

The Issue: Potential risk of brush detachment during cleaning. If brush detachment is...

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

Class II — Potential Health HazardOngoing
DrugApril 24, 2019· MAJOR PHARMACEUTICALS

Recalled Item: DIVALPROEX SODIUM EXTENDED-RELEASE TABLETS Recalled by MAJOR PHARMACEUTICALS...

The Issue: cGMP deviations: Product was exposed above 50% relative humidity levels...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 24, 2019· AVKARE Inc.

Recalled Item: Losartan Potassium Tablets USP 50 mg 50 tablets (5x10) Unit Recalled by...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 24, 2019· AVKARE Inc.

Recalled Item: Losartan Potassium Tablets USP 25 mg 50 tablets (5x10) Unit Recalled by...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 24, 2019· AmeriHerb International Inc

Recalled Item: Mullein leaf c/s Recalled by AmeriHerb International Inc Due to Potential E....

The Issue: Dried spice and herb products potentially contaminated with generic E. coli.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 24, 2019· AmeriHerb International Inc

Recalled Item: Blessed thistle herb c/s Recalled by AmeriHerb International Inc Due to...

The Issue: Dried spice and herb products potentially contaminated with generic E. coli.

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

Class II — Potential Health HazardOngoing
Refund