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. 2,486 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,486 in last 12 months

Showing 4270142720 of 51,768 recalls

Medical DeviceNovember 11, 2014· Heart Sync, Inc.

Recalled Item: ADULT Radiotranslucent Electrode Recalled by Heart Sync, Inc. Due to Heart...

The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 11, 2014· Ebi, Llc

Recalled Item: Solitaire-C Cervical Spacer System a) 14-531593 Drill/Awl Sleeve b)...

The Issue: A design deficiency was discovered whereby the Drill/Awl Sleeve and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2014· Heart Sync, Inc.

Recalled Item: ADULT Radiotransparent Electrode Recalled by Heart Sync, Inc. Due to Heart...

The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 11, 2014· Heart Sync, Inc.

Recalled Item: ADULT/CHILD Radiotranslucent Electrode Recalled by Heart Sync, Inc. Due to...

The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 11, 2014· Heart Sync, Inc.

Recalled Item: ADULT Radiotranslucent Electrode Recalled by Heart Sync, Inc. Due to Heart...

The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 11, 2014· Heart Sync, Inc.

Recalled Item: ADULT/CHILD Radiotransparent Electrode Recalled by Heart Sync, Inc. Due to...

The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 11, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to Printouts...

The Issue: Printouts may be printed in incorrect anatomical size when using syngo.plaza...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2014· Alcon Research, Ltd.

Recalled Item: Alcon Single-Use Curved Jewelers/Iris Bipolar Forceps Sterile RX Recalled by...

The Issue: The product is sold and labeled as EO sterilized, however the units were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2014· Cure Medical LLC

Recalled Item: Pediatric Recalled by Cure Medical LLC Due to Some of the intermediate boxes...

The Issue: Some of the intermediate boxes within lot 140417-3, were labeled as P8, a...

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

Class II — Potential Health HazardOngoing
DrugNovember 10, 2014· Reckitt Benckiser LLC

Recalled Item: Mucinex DM (guaifenesin 600mg and dextromethorphan HBr 30mg) Recalled by...

The Issue: Defective container: A customer complaint revealed the presence of a...

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

Class III — Low RiskOngoing
Refund
DrugNovember 10, 2014· Baxter Healthcare Corp.

Recalled Item: Potassium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...

The Issue: Labeling: Label Error On Declared Strength: Bags of Potassium Chloride 10...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 10, 2014· Riba Foods Inc

Recalled Item: Salpica 11.5 oz. Recalled by Riba Foods Inc Due to Undeclared Wheat

The Issue: Product may contain undeclared wheat.

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 10, 2014· Riba Foods Inc

Recalled Item: Salpica 16 oz. Jalapeno Jack Queso Dip Recalled by Riba Foods Inc Due to...

The Issue: Product may contain undeclared wheat.

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 10, 2014· Riba Foods Inc

Recalled Item: Salpica 8 oz. Black Bean Nacho Recalled by Riba Foods Inc Due to Undeclared...

The Issue: Product may contain undeclared wheat.

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 10, 2014· Riba Foods Inc

Recalled Item: Crate & Barrel 11.5 oz. Monterey Jack Queso Dip Recalled by Riba Foods Inc...

The Issue: Product may contain undeclared wheat.

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 10, 2014· Riba Foods Inc

Recalled Item: Arriba! 16 oz. Chili Con Queso-Hot Recalled by Riba Foods Inc Due to...

The Issue: Product may contain undeclared wheat.

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 10, 2014· Riba Foods Inc

Recalled Item: Salpica 8 oz. Ballpark Nacho Recalled by Riba Foods Inc Due to Undeclared Wheat

The Issue: Product may contain undeclared wheat.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 10, 2014· GE Inspection Technologies, LP

Recalled Item: GE Optional Laser Centering Device X-ray generator. Recalled by GE...

The Issue: GE has identified a potential failure to comply with 21 C.F.R. ¿ 1040.10 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2014· DePuy Orthopaedics, Inc.

Recalled Item: The ATTUNE INTUITION Impaction Handle is a re-useable instrument utilized...

The Issue: Complaints have indicated that the ATTUNE INTUITION Impaction Handle lever...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2014· DePuy Orthopaedics, Inc.

Recalled Item: Fixed Tibial bearing ATTUNE INTUITION Impactor The ATTUNE INTUITION...

The Issue: ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006)...

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

Class II — Potential Health HazardOngoing