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. 2,432 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,432 in last 12 months

Showing 4974149760 of 51,768 recalls

Medical DeviceSeptember 28, 2012· Ventana Medical Systems Inc

Recalled Item: VENTANA (a member of the Roche Group) DISCOVERY ULTRA Recalled by Ventana...

The Issue: Potential for a waste fluid overflow condition to accur while running...

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

Class II — Potential Health HazardOngoing
FoodSeptember 28, 2012· Fairytale Brownies, Inc

Recalled Item: Fairytale Brownies Brand Peanut Butter Cookies Recalled by Fairytale...

The Issue: The firm initiated voluntarily recall because the products contains peanut...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 28, 2012· Fairytale Brownies, Inc

Recalled Item: Fairytale Brand Peanut Butter Sprites Recalled by Fairytale Brownies, Inc...

The Issue: The firm initiated voluntarily recall because the products contains peanut...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 28, 2012· Fairytale Brownies, Inc

Recalled Item: Fairytale Brownies Brand Peanut Butter Brownies Recalled by Fairytale...

The Issue: The firm initiated voluntarily recall because the products contains peanut...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 28, 2012· Late July Snacks, LLC

Recalled Item: Late July Organic Mini Peanut Butter Sandwich Crackers packaged in Recalled...

The Issue: Organic Mini Peanut Butter Sandwich Crackers are recalled due to Sunland...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 28, 2012· Biomet 3i, LLC

Recalled Item: Product is Full OSSEOTITE 2 Tapered Certain Implant Recalled by Biomet 3i,...

The Issue: Biomet 3i recalled Full OSSEOTITE 2 Tapered Certain Implant and Full...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2012· Synthes USA HQ, Inc.

Recalled Item: Synthes External Fixation System Tube to Tube Clamp Recalled by Synthes USA...

The Issue: The insert provided with the product for the specific lot number indicates...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2012· ICU Medical, Inc.

Recalled Item: 3 PORT "OFF" MANIFOLD w/WASTE BAG Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical, Inc. has identified a potential comingling of components where...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2012· Biomet 3i, LLC

Recalled Item: Product is Full OSSEOTITE Parallel Walled Certain Implant Recalled by Biomet...

The Issue: Biomet 3i recalled Full OSSEOTITE 2 Tapered Certain Implant and Full...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2012· Encore Medical, Lp

Recalled Item: 6.5mm Cancellous Bone Screw Intended to be used for the Recalled by Encore...

The Issue: A product complaint was received where a size 20 screw was labeled as size...

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

Class II — Potential Health HazardOngoing
DrugSeptember 28, 2012· ITW Dymon

Recalled Item: Lemon Hand Sanitizing Wipes [n-alkyl dimethyl benzyl ammonium chloride...

The Issue: CGMP Deviations: The products were manufactured with raw material which...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 27, 2012· Fresenius Kabi USA, LLC

Recalled Item: ONDANSETRON INJECTION Recalled by Fresenius Kabi USA, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility: Glass vials may have finish fractures and...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2012· Genentech, Inc.

Recalled Item: CellCept (mycophenolate mofetil) capsules Recalled by Genentech, Inc. Due to...

The Issue: Short Fill: some bottles contained less than 120-count per labeled claim.

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

Class III — Low RiskOngoing
Refund
DrugSeptember 27, 2012· Dr. Reddy's Laboratories, Inc.

Recalled Item: Dr. Reddy's Quetiapine Fumarate Tablets Recalled by Dr. Reddy's...

The Issue: Failed USP Dissolution Test Requirements: During analysis of long term...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2012· Fresenius Kabi USA, LLC

Recalled Item: CYANOCOBALAMIN INJECTION Recalled by Fresenius Kabi USA, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility: Glass vials may have finish fractures and...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2012· Fresenius Kabi USA, LLC

Recalled Item: MIDAZOLAM HYDROCHLORIDE INJECTION Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Lack of Assurance of Sterility: Glass vials may have finish fractures and...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 27, 2012· Cellestis Inc

Recalled Item: VACUETTE Cellestis 1 ml QuantiFERON¿ - TB ANTIGEN Recalled by Cellestis Inc...

The Issue: Cellestis is recalling QuantiFERON¿¿ - TB Gold TB Blood Collection Tubes and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2012· Cellestis Inc

Recalled Item: Vacuette Cellestis 1 ml QuantiFERON¿ TB ANTIGEN (HA) High Altitude: Shake...

The Issue: Cellestis is recalling QuantiFERON¿¿ - TB Gold TB Blood Collection Tubes and...

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

Class II — Potential Health HazardOngoing
FoodSeptember 27, 2012· Newman's Own Organics

Recalled Item: Newman's Own Organics brand Newman-O's Peanut Butter Creme Filled Chocolate...

The Issue: The product was manufactured using peanut butter recalled by Sunland Inc....

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 27, 2012· Oregon Ice Cream, LLC

Recalled Item: Label reads in part "*** ORGANIC Alden's ICE CREAM PEANUT Recalled by Oregon...

The Issue: The products are being recalled because they contain peanut butter...

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

Class I — Serious Health HazardOngoing
Refund