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. 2,711 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,711 in last 12 months

Showing 2096120980 of 51,768 recalls

FoodOctober 31, 2019· Merical, LLC

Recalled Item: Leader Advanced Probiotic with 6 Probiotic Strains and 20 billion Recalled...

The Issue: Incorrect Probiotic blend indicated in the Supplemental Facts Panel on...

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

Class III — Low RiskOngoing
Refund
DrugOctober 30, 2019· Avantor Performance Materials Inc

Recalled Item: Potassium Phosphate Recalled by Avantor Performance Materials Inc Due to...

The Issue: Failed Stability Specifications: Product exceeds compendia and firm's...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 30, 2019· Teleflex Medical

Recalled Item: HUDSON RCI SHERIDAN SHERI-BRONCH Endobronchial Tube - Product Recalled by...

The Issue: The tracheal and brochial swivel connectors are incorrectly labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2019· Young Dental Manufacturing Co, LLC

Recalled Item: Oral-B Recalled by Young Dental Manufacturing Co, LLC Due to Product shelf...

The Issue: Product shelf life may be shorter than that indicated on the label.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2019· Allergan PLC

Recalled Item: XEN Gel Stent Recalled by Allergan PLC Due to Foreign Object Contamination

The Issue: Residual polishing compounds, that are used in the needle sleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2019· Bio-Signal Group Corp.

Recalled Item: HydroDot brand: Wave Prep 4 oz. tubes-Product 1710-03. An electroconductive...

The Issue: Product has the potential to be contaminated with Burkholderia cepacia (B....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2019· Bio-Signal Group Corp.

Recalled Item: HydroDot brand: Wave Prep Single use cups Recalled by Bio-Signal Group Corp....

The Issue: Product has the potential to be contaminated with Burkholderia cepacia (B....

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

Class II — Potential Health HazardOngoing
DrugOctober 28, 2019· Lannett Company, Inc.

Recalled Item: Lannett Ranitidine Syrup (Ranitidine Oral Solution Recalled by Lannett...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 28, 2019· Cardinal Health 200, LLC

Recalled Item: Genius 2 Tympanic Thermometer OEM Tympanic Item Code:303062 Recalled by...

The Issue: The frequency of calibration for the Genius Tympanic Thermometer as stated...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2019· Cardinal Health 200, LLC

Recalled Item: Genius 2 Tympanic Thermometer Private Label Item Code: 3069 Recalled by...

The Issue: The frequency of calibration for the Genius Tympanic Thermometer as stated...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2019· Cardinal Health 200, LLC

Recalled Item: Genius 2 Tympanic Thermometer (discontinued) Item Code: 303000 Recalled by...

The Issue: The frequency of calibration for the Genius Tympanic Thermometer as stated...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2019· Cardinal Health 200, LLC

Recalled Item: Genius 3 Tympanic Thermometer- electric thermometer Item Code: 303013...

The Issue: The frequency of calibration for the Genius Tympanic Thermometer as stated...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2019· Cardinal Health 200, LLC

Recalled Item: Genius 2 Tympanic Thermometer OEM Tympanic Item Code: 303063 Recalled by...

The Issue: The frequency of calibration for the Genius Tympanic Thermometer as stated...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Elecsys Anti-HAV IgM assay-for the in vitro qualitative detection of...

The Issue: Current software version of the Anti-HAV IgM APP-file (version 06.05-101)...

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

Class II — Potential Health HazardOngoing
DrugOctober 25, 2019· Novitium Pharma LLC

Recalled Item: Novitium Pharma Ranitidine Capsules 150 mg 500 capsules Rx Only Recalled by...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 25, 2019· Novitium Pharma LLC

Recalled Item: Novitium Pharma Ranitidine Capsules 150 mg 60 capsules Rx Only Recalled by...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 25, 2019· Novitium Pharma LLC

Recalled Item: Novitium Pharma Ranitidine Capsules 300 mg 30 capsules Rx Only Recalled by...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 25, 2019· Novitium Pharma LLC

Recalled Item: Novitium Pharma Ranitidine Capsules 300 mg 100 capsules Rx Only Recalled by...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 25, 2019· ICU Medical Inc

Recalled Item: 0.9% SODIUM CHLORIDE INJECTION Recalled by ICU Medical Inc Due to Presence...

The Issue: Presence of Particulate Matter.

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 25, 2019· ICU Medical Inc

Recalled Item: LACTATED RINGER'S Injection Recalled by ICU Medical Inc Due to Presence of...

The Issue: Presence of Particulate Matter.

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

Class I — Serious Health HazardOngoing
Refund