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.
Showing 41741–41760 of 51,768 recalls
Recalled Item: Raspberry Sorbet Recalled by Snoqualmie Gourmet Ice Cream Due to Potential...
The Issue: Raspberry Sorbet is being recalled due to the potential to be contaminated...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pear Ginger Sorbet Recalled by Snoqualmie Gourmet Ice Cream Due to Potential...
The Issue: Pear Ginger Sorbet is being recalled due to the potential to be contaminated...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Watermelon Sorbet Recalled by Snoqualmie Gourmet Ice Cream Due to Potential...
The Issue: Watermelon Sorbet is being recalled due to the potential to be contaminated...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Blueberry Ginger Sorbet Recalled by Snoqualmie Gourmet Ice Cream Due to...
The Issue: Blueberry Ginger Sorbet is being recalled due to the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: B-Lipo Recalled by Bethel Nutritional Consulting, Inc Due to Marketed...
The Issue: Marketed without an Approved NDA/ANDA; found to contain Lorcaserin, a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 3M ESPE Clinpro 5000 (1.1% Sodium Flouride) Recalled by 3M Company/3m Espe...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date - The subject lot is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SLIM-K Recalled by Bethel Nutritional Consulting, Inc Due to Marketed...
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD 10 mL Syringe BD Luer-Lok Tip with Blunt Plastic Cannula Recalled by...
The Issue: The stopper of the 10mL BD Luer-Lok syringe is not properly seated in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The MAYFIELD¿ Ultra 360 Base Unit for head positioner Recalled by Integra...
The Issue: Through an investigation of complaints, Integra found that there is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Cardiology ECG Management It is a software application designed...
The Issue: An ECG procedure time stamp is incorrect, due to a software error in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Revolution CT. Recalled by GE Healthcare Due to Potential...
The Issue: Potential safety issue due to a required torque check on three bolted joints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: lnline Persuader- PedFuse Pedicle Screw System Recalled by SpineFrontier,...
The Issue: A crack may develop in the handle to the Inline Persuader, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anti-Lambda APC-H7 Recalled by BD Biosciences, Systems & Reagents Due to Two...
The Issue: Two lots of the Anti-Lambda APC-H7 antibody are contaminated with CD38 antibody.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CD8 (Leu-2a) PE (In vitro diagnostic) Recalled by BD Biosciences, Systems &...
The Issue: One lot of CD8 PE is contaminated with CD4 FITC and may cause an unexpected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zippie Zone Pediatric Rigid Wheelchair Model EIRZ1. Recalled by Sunrise...
The Issue: There is the potential for the height adjustable handle to dislodge due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEPFLUSH-10 (HEPARIN LOCK FLUSH SOLUTION Recalled by Fresenius Kabi USA, LLC...
The Issue: The lot failed pH specification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quickie Q7 Adult Rigid Wheelchair Model EIR4. Recalled by Sunrise Medical...
The Issue: There is the potential for the height adjustable handle to dislodge due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINAC Accelerators: ARTISTE Recalled by Siemens Medical Solutions USA, Inc...
The Issue: A hardware update to replace the old PCB Assembly, Head Driver-G41 with PCB...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Focal Sim radiation therapy treatment planning system Recalled by Elekta,...
The Issue: Incorrect CT to ED when using the Monaco Image Statistics Tool.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Electric Pen Drive (EPD) System Recalled by Synthes, Inc. Due to In...
The Issue: In May 2013, the original recall was initiated due to complaints the Hand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.