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. 2,724 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,724 in last 12 months

Showing 1946119480 of 51,768 recalls

Medical DeviceApril 22, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS Pheno - Interventional Fluoroscopic X-Ray System Model: 10849000 -...

The Issue: If the C-arm leaves its intended travel path due to a fault within the...

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

Class II — Potential Health HazardOngoing
DrugApril 21, 2020· Sandoz, Inc

Recalled Item: Infuvite PEDiatric Pharmacy Recalled by Sandoz, Inc Due to Defective...

The Issue: Defective Container: Sub-optimal crimping in vial of Pediatric Infuvite...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 21, 2020· Bio-Rad Laboratories, Inc.

Recalled Item: BioPlex 2200 Syphilis Total & RPR Linked Immunoabsorption Assay Recalled by...

The Issue: The increased level of RPR reactivity in the BioPlex 2200 Syphilis Total &...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2020· Ion Beam Applications S.A.

Recalled Item: Proteus 235 The Proton Therapy System - Proteus 235 (brand Recalled by Ion...

The Issue: Signature from the user is necessary to proceed with specific actions in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2020· Philips North America, LLC

Recalled Item: Philips HeartStart XL Monitor/Defibrillators Model number: M4735A - Product...

The Issue: HeartStart XL MonitorlDefibrillators may not have been included in prior...

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

Class II — Potential Health HazardOngoing
DrugApril 20, 2020· Fresenius Kabi USA, LLC

Recalled Item: Ketorolac Tromethamine Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Presence of Particulate Matter - found in reserve sample vials at the firm.

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 20, 2020· Fresenius Kabi USA, LLC

Recalled Item: Ketorolac Tromethamine Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Presence of Particulate Matter - found in reserve sample vials at the firm.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2020· Glaxosmithkline Consumer Healthcare Holdings

Recalled Item: ChapStick Total Hydration Moisture + Tint + SPF15 Very Berry Recalled by...

The Issue: Labeling: Not elsewhere classified: Observed separation in the secondary...

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

Class III — Low RiskOngoing
Refund
DrugApril 20, 2020· Glaxosmithkline Consumer Healthcare Holdings

Recalled Item: ChapStick Total Hydration Moisture + Tint + SPF15 Pretty in Recalled by...

The Issue: Labeling: Not elsewhere classified: Observed separation in the secondary...

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

Class III — Low RiskOngoing
Refund
DrugApril 20, 2020· Glaxosmithkline Consumer Healthcare Holdings

Recalled Item: ChapStick Total Hydration Moisture + Tint + SPF15 Peachy Keen Recalled by...

The Issue: Labeling: Not elsewhere classified: Observed separation in the secondary...

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

Class III — Low RiskOngoing
Refund
DrugApril 20, 2020· Lupin Pharmaceuticals Inc.

Recalled Item: Lisinopril Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to Product...

The Issue: Product Mix-Up: a complaint received indicating mix-up of 10 mg Lisinopril...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 20, 2020· Ocean Spray Cranberries Inc.

Recalled Item: 5.5 oz cans of Ocean Spray Pink Lite Cranberry Juice Drink Recalled by Ocean...

The Issue: Product contains undeclared sulfites.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 20, 2020· Suntech Medical, Inc.

Recalled Item: Oscar 2 Recalled by Suntech Medical, Inc. Due to The device display, when...

The Issue: The device display, when activated, can show an incorrect decimal point when...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· ROi CPS LLC

Recalled Item: Regard. Item number: 830034. GS0348D- CVC Triple Lumen 20CM non Sulfa-Mercy....

The Issue: Custom procedure kits contains affected lots of PosiFlush Syringe, a product...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· Trividia Health, Inc.

Recalled Item: TRUE METRIX SELF MONITORING BLOOD GLUCOSE SYSTEM - Product Usage: Recalled...

The Issue: One (1) TRUE METRIX AIR blood glucose meter distributed in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· Philips North America, LLC

Recalled Item: Philips Sterilizable Defibrillator Internal Paddles - Internal paddles are...

The Issue: Internal Paddles may wear over time and may not be safe or ready for use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· Bovie Medical Corporation

Recalled Item: Renuvion/ J-Plasma Precise Handpiece. Catalog numbers BVX-150B Recalled by...

The Issue: Unexpected stress fractures on the shaft of the hand piece may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· Cardinal Health Inc.

Recalled Item: Professional Urine Drug Control Recalled by Cardinal Health Inc. Due to...

The Issue: Three products requiring storage conditions were incorrectly stored outside...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· Bovie Medical Corporation

Recalled Item: Renuvion/ J-Plasma Precise Open Handpiece. Catalog numbers BVX-044-BPS...

The Issue: Unexpected stress fractures on the shaft of the hand piece may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· Cardinal Health Inc.

Recalled Item: B-Hydroxybutyrate LiquiColor Recalled by Cardinal Health Inc. Due to Three...

The Issue: Three products requiring storage conditions were incorrectly stored outside...

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

Class II — Potential Health HazardOngoing