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. 2,798 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,798 in last 12 months

Showing 91819200 of 29,208 recalls

Medical DeviceAugust 24, 2021· Bard Peripheral Vascular Inc

Recalled Item: Catalog # BEK3411 Recalled by Bard Peripheral Vascular Inc Due to Due to...

The Issue: Due to misbranded products shipped to customers.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· National Distribution & Contracting Inc

Recalled Item: ECO 50TS Gel Tens Ultrasound 1in X 5L cube 1 Dispenser Btl Recalled by...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceAugust 24, 2021· National Distribution & Contracting Inc

Recalled Item: ECO 85CB Lotion Ultrasound 8.5 oz 24/cs ECO 40JBC Gel Recalled by National...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceAugust 24, 2021· Medtronic Perfusion Systems

Recalled Item: DLP Left Heart Vent Catheters Recalled by Medtronic Perfusion Systems Due to...

The Issue: Potential for a wire protrusion through the left heart vent catheter tip

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· Medtronic Perfusion Systems

Recalled Item: DLP Left Heart Vent Catheters Recalled by Medtronic Perfusion Systems Due to...

The Issue: Potential for a wire protrusion through the left heart vent catheter tip

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2021· Aesthetics Systems Usa Inc

Recalled Item: Action De Gala Recalled by Aesthetics Systems Usa Inc Due to Ultrasound gels...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceAugust 20, 2021· Microbiologics Inc

Recalled Item: SARS-CoV-2 Process Control (Pellet) - Product Usage: intended for use...

The Issue: The SARS-CoV-2 Process Control (Pellet) contains RNA transcripts that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2021· Greiner Bio-One North America, Inc.

Recalled Item: Greiner Bio-One VACUETTE¿ TUBE 2 ml 9NC Coagulation sodium citrate Recalled...

The Issue: Complaint of tubes clotting due to variation of anticoagulant and/or tubes...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2021· Microbiologics Inc

Recalled Item: SARS-CoV-2 Process Control (Swab) - Product Usage: intended for use Recalled...

The Issue: The product indicated is contaminated with a plasmid DNA that contains the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2021· Fort Defiance Industries, LLC

Recalled Item: P2131 Automated Field Steam Sterilizer NSN: 6530-01-641-4641 Recalled by...

The Issue: The rear heater plate and cover assembly that contains the electrical wiring...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2021· Philips Ultrasound Inc

Recalled Item: Philips Ultrasound Recalled by Philips Ultrasound Inc Due to Battery system...

The Issue: Battery system data issue with the ultrasound system can intermittently...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2021· Philips Ultrasound Inc

Recalled Item: Philips Ultrasound Recalled by Philips Ultrasound Inc Due to Battery system...

The Issue: Battery system data issue with the ultrasound system can intermittently...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2021· Scrip Inc

Recalled Item: Scrip Ultrasound Gel Clear Recalled by Scrip Inc Due to Ultrasound gels and...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceAugust 18, 2021· Scrip Inc

Recalled Item: Scrip Creme All Purpose Lotion Intended for use in acoustic Recalled by...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceAugust 18, 2021· Queen Comfort Products lLC

Recalled Item: COVENA PICC Sleeve Recalled by Queen Comfort Products lLC Due to Marketed...

The Issue: Marketed without FDA clearance

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Computed tomography x-ray systems with software syngo.CT VA20A_SP4a Recalled...

The Issue: Software versions may result in sporadic problems causing scanning workflow...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2021· In2bones USA, LLC

Recalled Item: CoLink Bone Graft Harvester Recalled by In2bones USA, LLC Due to Complaints...

The Issue: Complaints were received of CoLink Bone Graft Harvesters breaking at the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2021· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA BF-XT160 Bronchofibervideoscope Recalled by Olympus Corporation...

The Issue: A gluing step was not performed during the manufacturing of the affected...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2021· Olympus Corporation of the Americas

Recalled Item: BF-XP60 OES Bronchofiberscope Recalled by Olympus Corporation of the...

The Issue: The firm is issuing validated, new reprocessing instructions according to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2021· Biodex Medical Systems, Inc.

Recalled Item: Atomlab 500 Dose Calibrator Software 2.0.00 through Revision 2.0.08 Recalled...

The Issue: When deleting a previously entered custom isotope, the software deletes the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing