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 4354143560 of 51,768 recalls

Medical DeviceJuly 7, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Possible sound loss...

The Issue: Possible sound loss associated with the CARESCAPE Monitor B650. When an...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2014· Smiths Medical ASD, Inc.

Recalled Item: H4051 Endo Tube Holder Recalled by Smiths Medical ASD, Inc. Due to The tube...

The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 7, 2014· Smiths Medical ASD, Inc.

Recalled Item: H4002S Neonatal/Paed.Intubation Kit 3.0mm Murphy Recalled by Smiths Medical...

The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 7, 2014· Smiths Medical ASD, Inc.

Recalled Item: H4052 Endo Tube Holder Recalled by Smiths Medical ASD, Inc. Due to The tube...

The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 7, 2014· Smiths Medical ASD, Inc.

Recalled Item: H4002PS Neonatal/Paed.Intubation Kit 3.0mm Murphy Recalled by Smiths Medical...

The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 7, 2014· Smiths Medical ASD, Inc.

Recalled Item: 4001PS Neonatal/Paed.Intubation Kit 2.5mm Murphy Recalled by Smiths Medical...

The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 7, 2014· Smiths Medical ASD, Inc.

Recalled Item: H4001S Neonatal/Paed.Intubation Kit 2.5mm Murphy Recalled by Smiths Medical...

The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 7, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...

The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 3600 Immunodiagnostic System --- For use in the in vitro quantitative...

The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System --- For use in the in vitro quantitative...

The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2014· Innovasis, Inc

Recalled Item: Excella II Standard Pedicle Screw Recalled by Innovasis, Inc Due to Mislabeling

The Issue: Innovasis is recalling the Excella II Standard Pedicle Screw due to...

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

Class II — Potential Health HazardOngoing
DrugJuly 3, 2014· Mylan Pharmaceuticals Inc.

Recalled Item: Metoprolol Succinate Extended-release Tablets Recalled by Mylan...

The Issue: Presence of Foreign Tablets/Capsules: A pharmacist reported a rogue tablet...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 3, 2014· Fougera Pharmaceuticals Inc.

Recalled Item: Triamcinolone Acetonide Lotion USP Recalled by Fougera Pharmaceuticals Inc....

The Issue: Failed PH Specifications: It has been determined that the pH of the lots...

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

Class III — Low RiskOngoing
Refund
DrugJuly 3, 2014· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Diltiazem HCl Extended-release Capsules Recalled by Mylan Institutional,...

The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...

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

Class III — Low RiskOngoing
Refund
DrugJuly 3, 2014· Fougera Pharmaceuticals Inc.

Recalled Item: Triamcinolone Acetonide Lotion USP Recalled by Fougera Pharmaceuticals Inc....

The Issue: Failed PH Specifications: It has been determined that the pH of the lots...

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

Class III — Low RiskOngoing
Refund
FoodJuly 3, 2014· Metagenics, Inc.

Recalled Item: UltraBalance Protein Powder Recalled by Metagenics, Inc. Due to Undeclared Soy

The Issue: Metagenics is recalling UltraBalance Protein powder because it may contain...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 3, 2014· CooperSurgical, Inc.

Recalled Item: CooperSurgical H/S CATHETER (PART # 61-5007) Intended for Hysterosonography/...

The Issue: Unsealed pouches.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2014· Intelerad Medical Systems

Recalled Item: IntelePACS software versions 3-8-1 to 4-9-1 Recalled by Intelerad Medical...

The Issue: In specific situation a partially truncated file may be written to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas - In Line Valve only with SIPHONGUARD¿ Device Recalled by...

The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas - In Line Valve Only Recalled by Codman & Shurtleff, Inc. Due...

The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...

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

Class II — Potential Health HazardOngoing