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. 1,012 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
1,012 in last 12 months

Showing 36041–36060 of 51,768 recalls

Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Cardio software. Recalled by Merge Healthcare, Inc. Due to Cardio...

The Issue: Cardio study list does not show STAT studies without .

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: iConnect Enterprise Archive software. Recalled by Merge Healthcare, Inc. Due...

The Issue: The versions allow images to be stored without pixel data, resulting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: iConnect Enterprise Archive (ICEA) software. The firm name on the Recalled...

The Issue: An error message can occur resulting in the prior studies being unavailable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: iConnect Enterprise Archive (ICEA) software. iConnect Enterprise Archive is...

The Issue: The study is archived but cannot be opened in iConnect Access and cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Eye Care Systems Recalled by Merge Healthcare, Inc. Due to The system...

The Issue: The system will completely stop allowing the downloading or acquisition of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Eye Station Import Utility (ESIU). The firm name on Recalled by Merge...

The Issue: System locks up which may result in potential patient injury or delay in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: MasimoSET LNOP DCI adult SpO2 reusable sensor Recalled by Merge Healthcare,...

The Issue: Under certain conditions, the cables used with the Hemo system during a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Masimo SPO2 Sensor Recalled by Merge Healthcare, Inc. Due to Under certain...

The Issue: Under certain conditions, the cables used with the Hemo system during a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: MasimoSET LNOP DCIP pediatric/slender digit SpO2 reusable sensor Recalled by...

The Issue: Under certain conditions, the cables used with the Hemo system during a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: SpO2 connecting cable for Masimo LNCS sensor (Merge Part Number:...

The Issue: Under certain conditions, the cables used with the Hemo system during a...

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

Class II — Potential Health HazardOngoing
DrugApril 2, 2016· Complete Pharmacy and Medical Solutions LLC

Recalled Item: Human Chorionic Gonadotropin Recalled by Complete Pharmacy and Medical...

The Issue: Non-sterility - presence of bacteria confirmed by outside laboratory after...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 1, 2016· Platinum Distribution Inc

Recalled Item: R No Sugar Added Recalled by Platinum Distribution Inc Due to Manufacturer...

The Issue: Manufacturer Ross Chocolates, Coquitlam, BC Canada recalled these chocolate...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 1, 2016· Diamond Foods, Inc.

Recalled Item: Emerald 100 Calorie Packs of Cashew Halves & Pieces Recalled by Diamond...

The Issue: There is the potential for small glass fragments in Emerald 100 calorie...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 1, 2016· Sugarfina, LLC

Recalled Item: Sugarfina Chocolate Malt Balls Code 840278113565 SKU K1159 Recalled by...

The Issue: undeclared peanuts

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 1, 2016· Roland Foods, LLC.

Recalled Item: Roland (R) Fire Roasted Red Pepper Strips Recalled by Roland Foods, LLC. Due...

The Issue: Possible presence of glass fragments in the product lots.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 1, 2016· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Smart CR Digital Computed Radiography System Recalled by Fujifilm Medical...

The Issue: Reports of failure of the device's power supply.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. Passer....

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Applied Medical Resources Corp

Recalled Item: Direct Drive Clip Applier CA090 Recalled by Applied Medical Resources Corp...

The Issue: Increased customer complaints indicating inconsistent clip application; may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. Screw Recalled...

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. Fastener...

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing