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. 2,584 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,584 in last 12 months

Showing 3936139380 of 51,768 recalls

Medical DeviceJune 4, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Emotion 6 Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A potential safety issue involving two (2) broken screws and one (1) bowed,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Emotion 16 Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A potential safety issue involving two (2) broken screws and one (1) bowed,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2015· Volcano Corporation

Recalled Item: Prestige Plus 185cm J-Tip: Part number: 9185J Recalled by Volcano...

The Issue: During a relabeling procedure at the manufacturing facility, the products...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2015· Volcano Corporation

Recalled Item: Volcano PV .035 Catheter: Part number: 88901 Recalled by Volcano Corporation...

The Issue: During a relabeling procedure at the manufacturing facility, the products...

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

Class II — Potential Health HazardOngoing
DrugJune 3, 2015· Centro Naturista

Recalled Item: Smart Lipo Dietary Supplement capsules Recalled by Centro Naturista Due to...

The Issue: Marketed without an approved NDA/ANDA - Product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 3, 2015· Centro Naturista

Recalled Item: Smart Lipo Dietary Supplement capsules Recalled by Centro Naturista Due to...

The Issue: Marketed without an approved NDA/ANDA - Product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 3, 2015· Baxter Healthcare Corp

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

The Issue: Subpotent Drug; out of specification results for heparin raw material

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 3, 2015· Centro Naturista

Recalled Item: Smart Lipo Dietary Supplement capsules Recalled by Centro Naturista Due to...

The Issue: Multiple dietary supplement regulation violations.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 3, 2015· San Francisco Spice Company, Inc.

Recalled Item: Eating Right Black Bean Soup Recalled by San Francisco Spice Company, Inc....

The Issue: Some containers or Eating Right Black Bean Coup may contain Eating Right...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 3, 2015· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING FEMORAL HEAD Recalled by...

The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING ACETABULAR CUP W/IMPACTOR...

The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING DYSPLASIA CUP W/IMPACTOR...

The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Elite Biomedical Solutions LLC

Recalled Item: Alaris Medley LVP Frame Membrane. Intended use to hold platen Recalled by...

The Issue: Administration of inappropriate quantities of fluid can result, with the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2015· Elite Biomedical Solutions LLC

Recalled Item: Alaris Medley LVP Bezel Assembly. Intended use to hold platen Recalled by...

The Issue: Administration of inappropriate quantities of fluid can result, with the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to Error in...

The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to Error in...

The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 5-detector Recalled by Perkinelmer Due to Error in...

The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to Error in...

The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to Error in...

The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Perkinelmer

Recalled Item: WIZARD2 2-detector Recalled by Perkinelmer Due to Error in WIZARD2 Barcode...

The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results

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

Class II — Potential Health HazardOngoing