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. 2,665 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,665 in last 12 months

Showing 2272122740 of 51,768 recalls

DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: NEOSTIGMINE METHYL SULFATE 1MG/ML INJ SOL SYR Recalled by RXQ Compounding...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: EDETATE CALCIUM DISODIUM 150MG/ML INJECTABLE Recalled by RXQ Compounding LLC...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 19, 2019· UNFI General Corporate

Recalled Item: WOODSTOCK ORGANIC GRILLED RED PEPPER Recalled by UNFI General Corporate Due...

The Issue: Product tested positive for Listeria monocytogenes.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 19, 2019· Seca

Recalled Item: Seca 402/403 Baby Scale Cart Recalled by Seca Due to It has been determined...

The Issue: It has been determined that the wheels on the baby scale cart can...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Andover Healthcare Inc.

Recalled Item: Sterile Co-Flex Med 4" - Product Usage: Single Use secondary Recalled by...

The Issue: Incomplete packaging seal of sterile product

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Andover Healthcare Inc.

Recalled Item: Sterile Co-Flex NL 3" - Product Usage: Single Use secondary Recalled by...

The Issue: Incomplete packaging seal of sterile product

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Andover Healthcare Inc.

Recalled Item: Sterile Co-Flex LF2 3" - Product Usage: Single Use secondary Recalled by...

The Issue: Incomplete packaging seal of sterile product

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Andover Healthcare Inc.

Recalled Item: Sterile Co-Flex Med 3" - Product Usage: Single Use secondary Recalled by...

The Issue: Incomplete packaging seal of sterile product

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Andover Healthcare Inc.

Recalled Item: Sterile Co-Flex LF2 4" - Product Usage: Single Use secondary Recalled by...

The Issue: Incomplete packaging seal of sterile product

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Andover Healthcare Inc.

Recalled Item: Sterile Co-Flex NL 4" - Product Usage: Single Use secondary Recalled by...

The Issue: Incomplete packaging seal of sterile product

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Elekta, Inc.

Recalled Item: iGUIDE System with software build iGuide 2.2.0 Recalled by Elekta, Inc. Due...

The Issue: Potential for iGUIDE to incorrectly monitor the 3D position.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Pharmaceutical Innovations, Inc.

Recalled Item: ElectroMist product codes: 36-3310-25 - Product Usage: Electrode...

The Issue: Potential for failed stability antimicrobial effectiveness testing.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Pharmaceutical Innovations, Inc.

Recalled Item: Alpha Conducting solution product codes: 3310-25 ASCR - Product Usage:...

The Issue: Potential for failed stability antimicrobial effectiveness testing.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Pharmaceutical Innovations, Inc.

Recalled Item: ElectroMist product codes: 36-3310-60 - Product Usage: Electrode...

The Issue: Potential for failed stability antimicrobial effectiveness testing.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Pharmaceutical Innovations, Inc.

Recalled Item: ElectroMist product codes: 36-3310-04 - Product Usage: Electrode...

The Issue: Potential for failed stability antimicrobial effectiveness testing.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Pharmaceutical Innovations, Inc.

Recalled Item: Alpha Conducting solution product codes:3310-15 ACS - Product Usage:...

The Issue: Potential for failed stability antimicrobial effectiveness testing.

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

Class II — Potential Health HazardOngoing
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Droperidol Injectable Sterile Solution Recalled by Premier Pharmacy Labs Inc...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Brilliant Blue Ophthalmic PF INJ Recalled by Premier Pharmacy Labs Inc Due...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Neostigmine Methylsulfate Recalled by Premier Pharmacy Labs Inc Due to Lack...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: SUCCINYLcholine Chloride Recalled by Premier Pharmacy Labs Inc Due to Lack...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

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

Class II — Potential Health HazardOngoing
Refund