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. 2,612 recalls have been distributed to Washington in the last 12 months.
Showing 33061–33080 of 51,768 recalls
Recalled Item: MOZZARELLA LOW MOISTURE WHOLE MILK 8/6# DRAGONE Recalled by Saputo Cheese...
The Issue: Firm received one complaint from a food service customer stating a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MOZZARELLA SUPREME 8/6# CONTADINO Recalled by Saputo Cheese USA, Inc. Due to...
The Issue: Firm received one complaint from a food service customer stating a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Plush Puffs Marshmallows Toasty Coconut 4oz. and 2lb bulk bag Recalled by To...
The Issue: Undeclared allergen of milk from the declared ingredient coconut cream powder.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PROTONIX I.V. (pantoprazole sodium) for Injection Recalled by Pfizer Inc....
The Issue: Subpotent Drug: Out of Specification (OOS) for potency at the 6-month...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Toms of Maine Naturally Dry Natural Powder Antiperspirant Stick Recalled by...
The Issue: Labeling: Label Mix Up- Incorrect back label applied to the product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Black Widow Plate 19mm Plate Recalled by Amendia, Inc Due to There is a...
The Issue: There is a problem with the mating feature between the plate and screw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS IMMULITE 2000/2000 Xpi Systems Intact PTH (Parathyroid Hormone) Test...
The Issue: Siemens is conducting this recall for the IMMULITE¿ 2000/IMMULITE¿ 2000 XPi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Recalled by Teleflex Medical Due to Labeling Inconsistency: The...
The Issue: Labeling Inconsistency: The products have been labeled with the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Black Widow 6.6mm x 20mm Screw Recalled by Amendia, Inc Due to There is a...
The Issue: There is a problem with the mating feature between the plate and screw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Stylet Needle Recalled by Amendia, Inc Due to The rods are packaged in...
The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyberKnife Robotic Radiosurgery System using software version 10.6 Recalled...
The Issue: Accuray has become aware of a potential safety issue involving unexpected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Durex Pleasure Pack . 3 ultra fine lubricated latex condoms Recalled by...
The Issue: Reckitt Benckiser LLC is recalling Durex Condoms Pleasure Packs due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Savannah-T Straight Rod Recalled by Amendia, Inc Due to The rods are...
The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire 1.4mm x 12in Non-Threaded Recalled by Amendia, Inc Due to The rods...
The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G3 Opticage Expandable Interbody Fusion Device Recalled by Interventional...
The Issue: During implantation, the proximal end of the device could separate if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prestige II Recalled by GE Healthcare, LLC Due to GE Healthcare is...
The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prestige VH Recalled by GE Healthcare, LLC Due to GE Healthcare is...
The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTX LCA Recalled by GE Healthcare, LLC Due to GE Healthcare is...
The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Innova 2000 Recalled by GE Healthcare, LLC Due to GE Healthcare is...
The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Legacy Recalled by GE Healthcare, LLC Due to GE Healthcare is conducting a...
The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.