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. 2,486 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,486 in last 12 months

Showing 4310143120 of 51,768 recalls

FoodSeptember 5, 2014· Plum, Inc.

Recalled Item: Plum Organics Little Cremes: Organic Rice Milk Snacks Recalled by Plum, Inc....

The Issue: Increased number of complaints that product is not softening as intended and...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 5, 2014· Wholesome Harvest Baking, Inc.

Recalled Item: Frozen jalapeno bagels sold under the Maple Leaf Bakery brand Recalled by...

The Issue: Wholesome Harvest Baking, Inc. ("WHB"), formerly Maple Leaf Bakery, Inc., of...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 5, 2014· Mars Chocolate North America

Recalled Item: Twix Unwrapped Bites 7.0 oz. distributed by Mars chocolate na Recalled by...

The Issue: Mars Chocolate North is recalling Twix Brand Unwrapped Bites 7 oz. pouch due...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 5, 2014· Calavo Growers, Inc. (Corporate)

Recalled Item: Avocados Recalled by Calavo Growers, Inc. (Corporate) Due to Potential...

The Issue: Calavo Growers is recalling Avocados because they may be contaminated with...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 5, 2014· Zimmer Biomet, Inc.

Recalled Item: ROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled...

The Issue: The software issue described was corrected in the modification to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Precision 500D Recalled by GE Healthcare, LLC Due to GE...

The Issue: GE Healthcare has become aware of a potential safety issue involving missing...

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

Class II — Potential Health HazardOngoing
DrugSeptember 4, 2014· Hospira Inc.

Recalled Item: Bupivacaine HCl Inj. Recalled by Hospira Inc. Due to Presence of Particulate...

The Issue: Presence of Particulate Matter: A confirmed customer complaint reported the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 4, 2014· Midmark Corp dba Progeny Inc

Recalled Item: Vantage Panoramic X-Ray System used to perform dental and orthodontic...

The Issue: Failure of the primary collimator may result in unintentional movement of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2014· Teleflex Medical

Recalled Item: Rusch Recalled by Teleflex Medical Due to Misbranding: Although the product...

The Issue: Misbranding: Although the product labeling identifies the catheters as...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2014· Teleflex Medical

Recalled Item: Aqauapak 728 SW Recalled by Teleflex Medical Due to Possibility that the...

The Issue: Possibility that the nebulizer adaptor packaging may have open or weak seals...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2014· Teleflex Medical

Recalled Item: Aquapak Adaptor Recalled by Teleflex Medical Due to Possibility that the...

The Issue: Possibility that the nebulizer adaptor packaging may have open or weak seals...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2014· DePuy Orthopaedics, Inc.

Recalled Item: RECLAIM Distal Reamer Extension Non Sterile Intended as Recalled by DePuy...

The Issue: Specific lots are being recalled due to the potential for the tabs to break,...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Aerogen Ltd.

Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...

The Issue: Aerogen has received a small number of complaints in relation to the main...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Aerogen Ltd.

Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...

The Issue: Aerogen has received a small number of complaints in relation to the main...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Aerogen Ltd.

Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...

The Issue: Aerogen has received a small number of complaints in relation to the main...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Aerogen Ltd.

Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...

The Issue: Aerogen has received a small number of complaints in relation to the main...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens AXIOM Luminos dRF Max systems The Axiom Luminos dRF Recalled by...

The Issue: Two malfunctions posing potential risk to patients were identified with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Luminos Agile Max system The Luminos Agile is intended Recalled by...

The Issue: Two malfunctions posing potential risk to patients were identified with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Uroskop Omnia Max system The Uroskop Omnia is a Recalled by Siemens...

The Issue: Two malfunctions posing potential risk to patients were identified with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Ysio Max system The Ysio Max is a radiographic system used in...

The Issue: Two malfunctions posing potential risk to patients were identified with...

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

Class II — Potential Health HazardOngoing