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. 2,820 recalls have been distributed to Washington in the last 12 months.
Showing 4861–4880 of 51,768 recalls
Recalled Item: ACUSON Juniper 1.0 Recalled by Siemens Medical Solutions USA, Inc. Due to If...
The Issue: If ultrasound systems with software, are changed from factory default to :...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Creatine Kinase (CK) used on cobas c 311/501/502 and COBAS Recalled by Roche...
The Issue: Creatine Kinase (CK) Assay Abnormal calibrations on the cobas¿ c 311/501/502...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris EtCO2 Module Model 8300 Recalled by CareFusion 303, Inc. Due to Due...
The Issue: Due to affected devices that may have bent female IUI connector and may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SL BLOODLINE FOR FMC 2008 SERIES-Tubing to be used to Recalled by B Braun...
The Issue: Incomplete insertion of the patient connector of the Streamline Airless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Module Model 8100 Recalled by CareFusion 303, Inc. Due to Due to...
The Issue: Due to affected devices that may have bent female IUI connector and may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STREAMLINE FRESENIUS FOR DAVITA-Tubing to be used to transfer blood Recalled...
The Issue: Incomplete insertion of the patient connector of the Streamline Airless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STREAMLINE FRESENIUS FOR DAVITA-Tubing to be used to transfer blood Recalled...
The Issue: Incomplete insertion of the patient connector of the Streamline Airless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STREAMLINE BLOODLINE SET FOR DIALOG-Tubing to be used to transfer Recalled...
The Issue: Incomplete insertion of the patient connector of the Streamline Airless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STREAMLINE LONG-Tubing to be used to transfer blood between a Recalled by B...
The Issue: Incomplete insertion of the patient connector of the Streamline Airless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PCA Module Model 8120 Recalled by CareFusion 303, Inc. Due to Due to...
The Issue: Due to affected devices that may have bent female IUI connector and may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris System PC Unit Model 8015 - a modular infusion pump and monitoring...
The Issue: Due to affected devices that may have bent female IUI connector and may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Microalbumin_2 (¿ALB_2)-For in vitro diagnostic use in the...
The Issue: Atellica CH Microalbumin_2 (¿ALB_2) and the ADVIA Chemistry Microalbumin_2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Microalbumin_2 (¿ALB_2) -For in vitro diagnostic use in...
The Issue: Atellica CH Microalbumin_2 (¿ALB_2) and the ADVIA Chemistry Microalbumin_2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STREAMLINE BLOODLINE LONG VERSION Recalled by B Braun Medical Inc Due to...
The Issue: Incomplete insertion of the patient connector of the Streamline Airless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Syringe Module Model 8110 Recalled by CareFusion 303, Inc. Due to Due...
The Issue: Due to affected devices that may have bent female IUI connector and may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STREAMLINE BLOODLINE SET FOR DIALOG DR-Tubing to be used to Recalled by B...
The Issue: Incomplete insertion of the patient connector of the Streamline Airless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOW Real Foods Whole & Unsalted Raw Brazil Nuts 12oz. bag Recalled by Now...
The Issue: High mold, yeast, and total viable count
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TxHA PEEK IBF/TxTiHA IBF System i. TxHA The Recalled by Innovasis, Inc Due...
The Issue: Due to interfacing issues between the implant trial and inserter of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soltive Premium SuperPulsed Laser - Intended for incision Recalled by...
The Issue: The term Bladder Stone was incorrectly translated in both Spanish and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soltive Pro SuperPulsed Laser Systems-Intended for incision Recalled by...
The Issue: The term Bladder Stone was incorrectly translated in both Spanish and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.