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 29621–29640 of 51,768 recalls
Recalled Item: Albuterol Sulfate Inhalation Solution Recalled by Teva Pharmaceuticals USA...
The Issue: Failed Impurities/Degradation Specifications: high out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ArrowADVANTAGE 5 Pressure Injectable Peripherally Inserted Central Catheter...
The Issue: Finished good kits may contain incorrect components. Kits that should...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW PICC powered by ARROW VPS Stylet Recalled by Arrow International Inc...
The Issue: Finished good kits may contain incorrect components. Kits that should...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo Imaging version V31 (model # 10014063) is a Picture Recalled by...
The Issue: Siemens is releasing a letter to inform about potential data loss relevant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium VR DF4 1240 Recalled by Sorin Group Italia SRL - CRF Due to There...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew POLARSTEM(TM) Femoral Stems with Ti/HA (Standard Recalled by...
The Issue: The Cardan joint of the Polarstem Cardan could potentially fracture or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUOHY Epidural Needle Recalled by Epimed International Due to Potential for...
The Issue: Potential for partially incomplete seal of product, impacting sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium CRT DF1 1711 Recalled by Sorin Group Italia SRL - CRF Due to There...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium DR 1510 Recalled by Sorin Group Italia SRL - CRF Due to There is a...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium VR 1210 Recalled by Sorin Group Italia SRL - CRF Due to There is a...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COUDE Blunt Nerve Block Needle Recalled by Epimed International Due to...
The Issue: Potential for partially incomplete seal of product, impacting sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium DR DF4 1540 Recalled by Sorin Group Italia SRL - CRF Due to There...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium CRT-D 1741 Recalled by Sorin Group Italia SRL - CRF Due to There...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX-2 COUDE Epidural Needle Recalled by Epimed International Due to Potential...
The Issue: Potential for partially incomplete seal of product, impacting sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LaBri's Body Health XPLODE 30 capsules Exclusively distribute worldwide by...
The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LaBri's Body Health Atomic 60 Capsules Exclusively distributed worldwide by...
The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Famotidine Tablets USP Recalled by Teva Pharmaceuticals USA Due to Failed...
The Issue: Failed Tablet/Capsule Specification; out of specification for tablet weight
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Super Panther 7K Capsules 1250 mg blend Recalled by Chiavna Saffron LLC Due...
The Issue: Marketed without an Approved NDA/ANDA;FDA analysis found product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FUJINON ED-530XT. This device is intended for the visualization of Recalled...
The Issue: An update to the design and labeling was implemented to help reduce patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implant Direct Swish Duo-Grip Healing Collar Recalled by Implant Direct...
The Issue: The Swish Duo-Grip Healing Collar part number 9048-13H (4.8mm) package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.