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. 2,711 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,711 in last 12 months

Showing 2068120700 of 51,768 recalls

Medical DeviceDecember 3, 2019· GE Healthcare, LLC

Recalled Item: Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v17) bone densitometer...

The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2019· Johnson & Johnson Surgical Vision Inc

Recalled Item: Healon GV PRO 0.85 mL Recalled by Johnson & Johnson Surgical Vision Inc Due...

The Issue: Ophthalmic viscosurgical device may be difficult to remove from the eye,...

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

Class II — Potential Health HazardOngoing
DrugDecember 2, 2019· AuroMedics Pharma LLC

Recalled Item: Moxifloxacin Ophthalmic Solution USP Recalled by AuroMedics Pharma LLC Due...

The Issue: Discoloration: Market complaints of discoloration in Moxifloxacin Ophthalmic...

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

Class III — Low RiskOngoing
Refund
DrugDecember 2, 2019· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Amantadine Hydrochloride Tablets Recalled by Jubilant Cadista...

The Issue: Presence of Foreign Substance: Presence of a foreign object in a single tablet.

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 2, 2019· Dole Fresh Vegetables Inc

Recalled Item: Tri-Color Coleslaw - Marketside brand Recalled by Dole Fresh Vegetables Inc...

The Issue: Canadian Food Inspection Agency reported finding Salmonella in a sample of...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 2, 2019· CornFusion Gourmet Popcorn, LLC

Recalled Item: Caramel flavored Popcorn Recalled by CornFusion Gourmet Popcorn, LLC Due to...

The Issue: Butter (cream) is declared but milk is not declared on label.

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 2, 2019· CornFusion Gourmet Popcorn, LLC

Recalled Item: Maple Bacon flavored Popcorn Recalled by CornFusion Gourmet Popcorn, LLC Due...

The Issue: Butter (cream) is declared but milk is not declared on label.

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 2, 2019· CornFusion Gourmet Popcorn, LLC

Recalled Item: Caramel Apple flavored Popcorn Recalled by CornFusion Gourmet Popcorn, LLC...

The Issue: Butter (cream) is declared but milk is not declared on label.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 2, 2019· 3-D Matrix, Inc.

Recalled Item: PuraSinus Absorbable Nasal Hemostat Recalled by 3-D Matrix, Inc. Due to The...

The Issue: The boxes used by the shipper were not validated for use during transport.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· Argon Medical Devices, Inc

Recalled Item: BioPince Full Core Biopsy Instrument 16ga x 15cm. Recalled by Argon Medical...

The Issue: Incorrect product labeling.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· Polymer Technology Systems, Inc.

Recalled Item: PTS Diagnostics CardioChek Plus Professional Analyzer Recalled by Polymer...

The Issue: One brand of batteries have a small dimensional difference in the negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· Polymer Technology Systems, Inc.

Recalled Item: Henry Schein CardioChek Starter Kit Recalled by Polymer Technology Systems,...

The Issue: One brand of batteries have a small dimensional difference in the negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· Polymer Technology Systems, Inc.

Recalled Item: PTS Diagnostics CardioChek Plus Professional Analyzer Recalled by Polymer...

The Issue: One brand of batteries have a small dimensional difference in the negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· Polymer Technology Systems, Inc.

Recalled Item: Henry Schein CardioChek Plus Professional Analyzer Recalled by Polymer...

The Issue: One brand of batteries have a small dimensional difference in the negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· Medical Action Industries, Inc. 306

Recalled Item: Medical convenience trays and kits Recalled by Medical Action Industries,...

The Issue: The kits contain a bottle of saline solution which may exceed the USP...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· Thoratec Corp.

Recalled Item: HeartMate 3 Mobile Power Unit Recalled by Thoratec Corp. Due to Excessive...

The Issue: Excessive static electricity can potentially cause unrecoverable power loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· Medela Inc

Recalled Item: Invia Foam Dressing Kit with FitPad - X-Large (3 pcs) Recalled by Medela Inc...

The Issue: Invia Foam Dressing Kit with FitPad could have holes in the sterile packaging.

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

Class II — Potential Health HazardOngoing
DrugNovember 27, 2019· Pfizer Inc.

Recalled Item: 25% Dextrose Injection Recalled by Pfizer Inc. Due to Labeling: Incorrect or...

The Issue: Labeling: Incorrect or Missing Lot and/or expiration date.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 27, 2019· Flexicare Medical Ltd.

Recalled Item: BriteBlade Pro Single-Use Fiber Optic Handle and Blade Mac 3 Recalled by...

The Issue: The firm has received reports that the spring/washer/bearing components in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2019· Flexicare Medical Ltd.

Recalled Item: BriteBlade Pro Single-se Fiber Optic Miller 2 Recalled by Flexicare Medical...

The Issue: The firm has received reports that the spring/washer/bearing components in...

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

Class II — Potential Health HazardOngoing