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. 1,777 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
1,777 in last 12 months

Showing 4780147820 of 51,768 recalls

Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments 0400-850-100 T5 zipper Toga with Peel Away Recalled by...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Prism Medical Services USA

Recalled Item: BC Hammock Mesh Sling (Small) Recalled by Prism Medical Services USA Due to...

The Issue: The product does not meet the firm's size standards, the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments 0400-830-000 T4 Toga Recalled by Stryker Instruments...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments0400-750-000 T4 Toga Recalled by Stryker Instruments Div....

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments 0400-710-000 T4 Pullover Toga (S/M) Sterile Recalled by...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments 0400-850-000S2 T4 Toga Recalled by Stryker Instruments...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments 0400-820-000S3 T4 Toga w/Inside Shoulder Ties Recalled...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Prism Medical Services USA

Recalled Item: BC Hammock Mesh Sling (Medium) Recalled by Prism Medical Services USA Due to...

The Issue: The product does not meet the firm's size standards, the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Prism Medical Services USA

Recalled Item: BC Hammock Mesh Sling (Large) Recalled by Prism Medical Services USA Due to...

The Issue: The product does not meet the firm's size standards, the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Pinook-Usa

Recalled Item: Pinook Mini Massager Distributed by www.pinookusa.com. Used to strengthen...

The Issue: Failure to submit a premarket submission and gain approval of a medical device.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Pinook-Usa

Recalled Item: Pinook Micro Massager Distributed by www.pinookusa.com Used to strengthen...

The Issue: Failure to submit a premarket submission and gain approval of a medical device.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Zimmer, Inc.

Recalled Item: Bigliani/Flatow¿ The Complete Solution Fukuda Retractors Small Nonsterile...

The Issue: This is a recall expansion from the 2010 recall which now includes seven...

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

Class II — Potential Health HazardOngoing
FoodMay 23, 2013· Mother Earth International LLC

Recalled Item: Mother Earth Products Recalled by Mother Earth International LLC Due to...

The Issue: The product was manufactured with a Soy Protein Isolate manufactured by CHS,...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 22, 2013· Florida Nutri Labs, LLC

Recalled Item: "***DIETARY SUPPLEMENT 4HB STACK Bedtime***52 CAPLETS***MANUFACTURED...

The Issue: Customer reported that a product user complained that the caplets were not...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 22, 2013· Florida Nutri Labs, LLC

Recalled Item: "***DIETARY SUPPLEMENT 4HB STACK Mealtime***78 CAPLETS***MANUFACTURED...

The Issue: Customer reported that a product user complained that the caplets were not...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 22, 2013· Elekta, Inc.

Recalled Item: Monaco RTP System Radiation Therapy Treatment Planning System. Radiation...

The Issue: Patient needs to be positioned as indicated by the treatment plan.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2013· Baxter Healthcare Corp.

Recalled Item: Baxter Recalled by Baxter Healthcare Corp. Due to leaking pouches

The Issue: leaking pouches

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

Class II — Potential Health HazardOngoing
DrugMay 21, 2013· Baxter Healthcare Corp.

Recalled Item: Heparin Sodium and 0.9% Sodium Chloride Injection Recalled by Baxter...

The Issue: Lack of Assurance of Sterility: Specific lot numbers of these products have...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 21, 2013· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...

The Issue: Lack of Assurance of Sterility: Specific lot numbers of these products have...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 21, 2013· American Health Packaging

Recalled Item: Zolpidem Tartrate Tablets 5 mg Recalled by American Health Packaging Due to...

The Issue: Unit Dose Mispackaging: This recall event is due to a random undetected...

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

Class II — Potential Health HazardOngoing
Refund