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. 2,698 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,698 in last 12 months

Showing 2166121680 of 51,768 recalls

Medical DeviceAugust 30, 2019· Philips Ultrasound Inc

Recalled Item: Transducer S8-3t UDI (01)00884838073524 Can be used as Recalled by Philips...

The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2019· Philips Ultrasound Inc

Recalled Item: Transducer S7-3t UDI (01)00884838061439 Can be used with: Recalled by...

The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2019· Philips Ultrasound Inc

Recalled Item: Transducer S8-3t UDI (01)00884838067523 Can be used with: Recalled by...

The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2019· Philips Ultrasound Inc

Recalled Item: Transducer S7-3t UDI (01)00884838067530 Used as accessory with: Recalled by...

The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2019· Pajunk GmbH

Recalled Item: SPROTTE Lumbar with Introducer Recalled by Pajunk GmbH Due to Problem with...

The Issue: Problem with packaging sealing process which affects sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2019· GE Healthcare, LLC

Recalled Item: ApexPro Telemetry Server System. Also identified as Modification To: ApexPro...

The Issue: May not provide visual and/or audible alarms at the CARESCAPE Central...

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

Class II — Potential Health HazardOngoing
DrugAugust 29, 2019· Johnson Matthey Inc.

Recalled Item: Fentanyl Citrate Active Pharmaceutical Ingredient Recalled by Johnson...

The Issue: cGMP Deviations: Potential glass contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 29, 2019· Johnson Matthey Inc.

Recalled Item: Cisplatin Active Pharmaceutical Ingredient Recalled by Johnson Matthey Inc....

The Issue: cGMP Deviations: Potential glass contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 29, 2019· Johnson Matthey Inc.

Recalled Item: Oxaliplatin Active Pharmaceutical Ingredient Recalled by Johnson Matthey...

The Issue: cGMP Deviations: Potential glass contamination

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 29, 2019· LABSTYLE INNOVATIONS

Recalled Item: Dario Blood Glucose Monitoring System Recalled by LABSTYLE INNOVATIONS Due...

The Issue: The Dario-Blood Glucose Tracker Android App versions 4.3.0-4.3.2 may...

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

Class II — Potential Health HazardOngoing
DrugAugust 28, 2019· AVKARE Inc.

Recalled Item: AVKARE Fexofenadine Hydrochloride Tablets USP Antihistamine 180 mg Recalled...

The Issue: Failed Stability Specifications.

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 28, 2019· Jivan Shakti Inc.

Recalled Item: Plastic Bottles labeled with: "Ancient Youth Secret - Since 500 B.C....

The Issue: Product label declares Vitamin D3 at 200 IU per serving. FDA sample analysis...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 28, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion CIRCLAMP W/1.3 CM BELL-single-use Recalled by Centurion Medical...

The Issue: A mismatch between the angle of the hole in the base and the angle of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: cobas c 701 and 702 Analyzer/Module-RF interference claims for the Recalled...

The Issue: Tina-quant Soluble Transferrin Receptor (STFR) Assays Updated Claims for...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion CIRCLAMP W/1.1CM BELL - single-use Recalled by Centurion Medical...

The Issue: A mismatch between the angle of the hole in the base and the angle of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: cobas c 311 Recalled by Roche Diagnostics Operations, Inc. Due to Tina-quant...

The Issue: Tina-quant Soluble Transferrin Receptor (STFR) Assays Updated Claims for...

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

Class II — Potential Health HazardOngoing
DrugAugust 27, 2019· American Health Packaging

Recalled Item: Lamivudine Tablets Recalled by American Health Packaging Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Package Insert; an error in the Dosage Forms...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 27, 2019· Karl Storz Endoscopy

Recalled Item: Karl Storz NEURO-FIBERSCOPE Recalled by Karl Storz Endoscopy Due to During a...

The Issue: During a complaint investigation it was determined that an error was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2019· Karl Storz Endoscopy

Recalled Item: Karl Storz RHINO-LARYNGO-BRONCHO FIBERSCOPE Recalled by Karl Storz Endoscopy...

The Issue: During a complaint investigation it was determined that an error was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2019· Karl Storz Endoscopy

Recalled Item: Karl Storz Recalled by Karl Storz Endoscopy Due to During a complaint...

The Issue: During a complaint investigation it was determined that an error was...

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

Class II — Potential Health HazardOngoing