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. 2,765 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,765 in last 12 months

Showing 1518115200 of 51,768 recalls

Medical DeviceSeptember 17, 2021· Bio-Rad Laboratories, Inc.

Recalled Item: BIO-RAD BioPlex 2200 Syphilis Total & RPR Calibrator Recalled by Bio-Rad...

The Issue: Due to two issues: 1) Customer complaints associated with greater than...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2021· Bio-Rad Laboratories, Inc.

Recalled Item: BIO-RAD BioPlex 2200 SYPH T PACK Syphilis Total Recalled by Bio-Rad...

The Issue: Due to two issues: 1) Customer complaints associated with greater than...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2021· Elekta, Inc.

Recalled Item: Elekta Medical Linear Accelerator (EMLA) Recalled by Elekta, Inc. Due to...

The Issue: There is a risk that the Diode D1 in the Modulator can fail in a destructive...

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

Class II — Potential Health HazardOngoing
FoodSeptember 16, 2021· The Earl of Sandwiches

Recalled Item: Earle of Sandwiches Mild Smoked Jalapeno Sub Recalled by The Earl of...

The Issue: Sandwiches may contain undeclared soy and egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 16, 2021· The Earl of Sandwiches

Recalled Item: Duke of Earle Spicy Chicken Sub Recalled by The Earl of Sandwiches Due to...

The Issue: Sandwiches may contain undeclared soy and egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 16, 2021· The Earl of Sandwiches

Recalled Item: Earle of Sandwiches X-Large Roast Beef Italiano Recalled by The Earl of...

The Issue: Sandwiches may contain undeclared egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 16, 2021· The Earl of Sandwiches

Recalled Item: Duke of Earle X-Large Ham & Cheese Recalled by The Earl of Sandwiches Due to...

The Issue: Sandwiches may contain undeclared soy and egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 16, 2021· The Earl of Sandwiches

Recalled Item: Earle of Sandwiches X-Large Oven Roasted Turkey Recalled by The Earl of...

The Issue: Sandwiches may contain undeclared soy and egg.

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 15, 2021· American Health Packaging

Recalled Item: Valproic Acid Oral Solution Recalled by American Health Packaging Due to...

The Issue: CGMP Deviations: Potential concern with products manufactured using liquid...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 14, 2021· Bayer Medical Care, Inc.

Recalled Item: The MEDRAD Twist & Go Disposable Syringe 150 mL with Recalled by Bayer...

The Issue: Labeling error: MEDRAD Mark 7 Arterion Injection System Syringes (ART 700...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2021· Elekta Inc

Recalled Item: Elekta Monaco - Product Usage: used to make treatment plans Recalled by...

The Issue: Contour changes can be saved on an unintended image set. In addition, these...

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

Class II — Potential Health HazardOngoing
DrugSeptember 13, 2021· Viatris

Recalled Item: Candesartan Cilexetil Tablets Recalled by Viatris Due to Failed...

The Issue: Failed Impurities/Degradation Specifications; out of specification for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 13, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic Bio-Medicus Insertion Kits Recalled by Medtronic Perfusion Systems...

The Issue: There was a label mix-up between two model numbers resulting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2021· Innovative Orthopedic Technologies, LLC

Recalled Item: ARCH Leg Positioning System Recalled by Innovative Orthopedic Technologies,...

The Issue: Due to the holes not being bored to the specific diameter, the locking pins...

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

Class II — Potential Health HazardOngoing
DrugSeptember 10, 2021· Piramal Critical Care, Inc.

Recalled Item: Rocuronium Bromide Injection 50mg/5 mL Recalled by Piramal Critical Care,...

The Issue: Labeling: Label Lacks Warning or Rx Legend: Finished product did not include...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 10, 2021· Karl Storz Endoscopy

Recalled Item: FIVE S 3.5x65 Recalled by Karl Storz Endoscopy Due to During a regular...

The Issue: During a regular requalification review, affected flexible intubation video...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2021· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: Foundation Kit Recalled by Stradis Medical, LLC dba Stradis Healthcare Due...

The Issue: Firm unable to confirm that the tenaculum devices were produced in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2021· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: IUD Insertion Pack Recalled by Stradis Medical, LLC dba Stradis Healthcare...

The Issue: Firm unable to confirm that the tenaculum devices were produced in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2021· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: IUD Insertion Kit Recalled by Stradis Medical, LLC dba Stradis Healthcare...

The Issue: Firm unable to confirm that the tenaculum devices were produced in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2021· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: Tenaculum Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...

The Issue: Firm unable to confirm that the tenaculum devices were produced in...

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

Class II — Potential Health HazardOngoing