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. 2,624 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,624 in last 12 months

Showing 2740127420 of 51,768 recalls

Medical DeviceApril 20, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.Now Recalled by Siemens Medical Solutions USA, Inc Due to There...

The Issue: There is a potential for a software issue that may cause the need for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Gentamicin Flex reagent cartridge Recalled by Siemens Healthcare...

The Issue: The affected lots may exhibit inaccuracy for Quality Control and patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2018· MicroAire Surgical Instruments, LLC

Recalled Item: MicroAire SmartRelease Endoscopic System Recalled by MicroAire Surgical...

The Issue: The Instructions for Use (IFU) is incorrect with regards to sterilization...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2018· Maquet SAS

Recalled Item: VOLISTA StandOP (model 600) surgical lights shipped from October 2012...

The Issue: Potential keypad failure on VOLISTA StandOP Surgical Lights.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Gentamicin Flex reagent cartridge Recalled by Siemens...

The Issue: The affected lots may exhibit inaccuracy for Quality Control and patient...

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

Class II — Potential Health HazardOngoing
DrugApril 19, 2018· Sun Pharmaceutical Industries, Inc.

Recalled Item: Sulfamethoxazole and Trimethoprim Tablets USP Recalled by Sun Pharmaceutical...

The Issue: Presence of Foreign Substance:Sun Pharma is recalling one (1) lot of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodApril 18, 2018· Viable Solutions, LLC

Recalled Item: Mitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyna Speciosa...

The Issue: Mitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyna Speciosa Leaf...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodApril 18, 2018· Viable Solutions, LLC

Recalled Item: Mitragyna Speciosa Leaf Powder-GREEN Horn Recalled by Viable Solutions, LLC...

The Issue: Mitragyna Speciosa Leaf Powder Green Horn Kratom product is being recalled...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodApril 18, 2018· Viable Solutions, LLC

Recalled Item: Mitragyna Speciosa Leaf Powder-Thai Maeng Da Recalled by Viable Solutions,...

The Issue: Mitragyna Speciosa Leaf Powder Thai Maeng Da Kratom product is being...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodApril 18, 2018· NatureBox, Inc.

Recalled Item: Whole Wheat Chocolate Animal Cookies Recalled by NatureBox, Inc. Due to...

The Issue: While packing from a bulk bin of whole wheat chocolate animal cookies, 2...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2018· Rhodes Pharmaceuticals, L.P.

Recalled Item: Aptensio XR (methylphenidate HCl extended-release) capsules 15 mg Rx Only...

The Issue: Failed Dissolution Specification: Low dissolution outside of specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceApril 17, 2018· Gyrus Acmi, Incorporated

Recalled Item: Gyrus ACMI Reusable Active Cord for Bovie/ValleyLab Generators Recalled by...

The Issue: There is a potential for the cord to spark and cause a fire.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Quadra Assura Recalled by St Jude Medical Inc. Due to The firm is releasing...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Fortify Assura Recalled by St Jude Medical Inc. Due to The firm is releasing...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Unify Quadra Recalled by St Jude Medical Inc. Due to The firm is releasing...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Quadra Assura MP Recalled by St Jude Medical Inc. Due to The firm is...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Fortify Recalled by St Jude Medical Inc. Due to The firm is releasing new...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Unify Assura Recalled by St Jude Medical Inc. Due to The firm is releasing...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· Bard Peripheral Vascular Inc

Recalled Item: BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter Recalled by...

The Issue: Device is at risk of having detectable levels of bacterial endotoxin present...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· Cook Inc.

Recalled Item: Advance¿ 35LP Low-Profile PTA Balloon Dilatation Catheter Recalled by Cook...

The Issue: Incorrect product labeling. Product labeled as 6mm x 2cm balloon are...

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

Class II — Potential Health HazardOngoing