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. 2,469 recalls have been distributed to Washington in the last 12 months.
Showing 44881–44900 of 51,768 recalls
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Models: M3535A and M3536A with...
The Issue: When the HeartStart MRx.is used with the Q-CPR Meter in defibrillation mode,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Model numbers: M3535A Recalled...
The Issue: MRx may display a Red X in the Ready For Use (RFU) indicator during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defibrillator Recalled by Philips Medical Systems,...
The Issue: A component of the MRx Processor Board may be susceptible to damage from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Defibrillator/Monitor M3538A Lithium Ion Batteries Revision J...
The Issue: Philips HeartStart MRx Monitor/Defibrillator, when operating on battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Recalled by Philips Medical...
The Issue: ECG trunk cable and connector block of the MRx could be susceptible to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XiO RPT System The XiO RTP System is used to Recalled by Elekta, Inc. Due to...
The Issue: Dose and Monitor Unit values are not computed correctly when Elekta...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CITRULLINE (L) in 25 g Recalled by Medisca Inc Due to Labeling: Label...
The Issue: Labeling: Label Mix-Up: FDA tested samples of API from Medisca, labeled as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetylcysteine Solution Recalled by Ben Venue Laboratories Inc Due to...
The Issue: Presence of Particulate Matter: During a review of retain samples, the firm...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluoxetine Capsules Recalled by Legacy Pharmaceutical Packaging Due to...
The Issue: Chemical Contamination: The recalling firm received notice that their...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: etomidate injection Recalled by Agila Specialties Private Ltd. Due to...
The Issue: Presence of Particulate Matter: Potential for small black particles to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RaySearch Ray Station Radiation Therapy Treatment Planning System Recalled...
The Issue: RaySearch Laboratories has recalled "RaySearch Ray Station 2.0, 2.5, 3.0,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs Healthcare G2 Clinical Access Mislabeled CDs for PN: 063-1829-11...
The Issue: Spacelabs has voluntarily recalled G2 Clinical Access Software CD because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CT580/Discovery CT590RT scanners running software...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Device Name: ABX PENTRA ML Model/Part #(s): A11A01652 Lot/Serial #(s):...
The Issue: HORIBA Medical initiated this recall of all software versions of ABX PENTRA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL Recalled by Philips Medical Systems, Inc. Due to...
The Issue: Philips HeartStart XL may experience a power board failure causing failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Other Macaroon G'nache P'nache 5.3 oz. Manufactured and Distributed...
The Issue: Northern Valley Baking Company did not declare milk or soy on the allergen...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bakes Sea Salt Potato Chips Recalled by Diamond Foods Inc Due to Undeclared Milk
The Issue: Kettle Foods, Inc. is recalling Bakes Sea Salt Potato Chips, Kettle Brand,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VerifyNow IIb/IIIa Test Recalled by Accumetrics Inc Due to Accumetrics is...
The Issue: Accumetrics is recalling the VerifyNow IIb/IIIa test because it may result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.