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. 2,665 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,665 in last 12 months

Showing 2262122640 of 51,768 recalls

Medical DeviceJune 21, 2019· Alto Development Corp

Recalled Item: A&E Medical Corp. Ultra-Flex MYO/Wire Ultra-Flex Monopolar Pacing Wire...

The Issue: Updated instructions for use: Ultra-Flex MYO/WIRE Monopolar pacing wire...

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

Class II — Potential Health HazardOngoing
DrugJune 20, 2019· Macleods Pharma Usa Inc

Recalled Item: Losartan Potassium Tablets 50 mg 1000 Tablets Recalled by Macleods Pharma...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2019· Macleods Pharma Usa Inc

Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by Macleods...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2019· Macleods Pharma Usa Inc

Recalled Item: Losartan Potassium Tablets Recalled by Macleods Pharma Usa Inc Due to CGMP...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2019· Macleods Pharma Usa Inc

Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by Macleods...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2019· Macleods Pharma Usa Inc

Recalled Item: Losartan Potassium andHydrochlorothiazide Tablets 100 mg/25 mg 90 tablets...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 20, 2019· Tropical Nut & Fruit Company

Recalled Item: Truly Good Foods Edamame Beans Roasted and Salted 7 oz. Recalled by Tropical...

The Issue: Allergen statement not printed on label of roasted and salted Edamame

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 20, 2019· Perrigo Company PLC

Recalled Item: Parent's Choice Advantage Infant Formula Milk-Based Powder with Iron...

The Issue: Product may contain metal fragments.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 20, 2019· Cincinnati Sub-Zero Products LLC, a Gentherm Company

Recalled Item: Norm-O-Temp model 111Z Recalled by Cincinnati Sub-Zero Products LLC, a...

The Issue: The manual does not provide instruction stating that exceeding 40 Celsius...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2019· Cincinnati Sub-Zero Products LLC, a Gentherm Company

Recalled Item: Norm-O-Temp model 111W Recalled by Cincinnati Sub-Zero Products LLC, a...

The Issue: The manual does not provide instruction stating that exceeding 40 Celsius...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2019· St Jude Medical Inc.

Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...

The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 20, 2019· St Jude Medical Inc.

Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...

The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 20, 2019· St Jude Medical Inc.

Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...

The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 20, 2019· St Jude Medical Inc.

Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...

The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 20, 2019· St Jude Medical Inc.

Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...

The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 20, 2019· St Jude Medical Inc.

Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...

The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...

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

Class I — Serious Health HazardOngoing
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: TURBO DROPS (PHEN 10% / CYCLO 1%/ TROP 1%/ KETO 0.5%) OPHTH SOLN Recalled by...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: HYDROXOCOBALAMIN 1000 MCG/ML (MDV) Recalled by RXQ Compounding LLC Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: KETAMINE 10 MG/ML INJ SOL SYR (C-III) Recalled by RXQ Compounding LLC Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: TURBO CAINE 2.5 (PHEN2.5/CYCLO1/ TROP1/TETRA 0.5) Recalled by RXQ...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund