Product Recalls in Idaho

Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,407 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
2,407 in last 12 months

Showing 2342123440 of 27,833 recalls

Medical DeviceJuly 10, 2014· Medical Positioning Inc

Recalled Item: Medical Positioning Rapid Response HUT table with Dual 2 Way Drop Section...

The Issue: Excessive weight on the table will cause tables with the affected component...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2014· Medical Positioning Inc

Recalled Item: Medical Positioning Rapid Response HUT table Recalled by Medical Positioning...

The Issue: Excessive weight on the table will cause tables with the affected component...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2014· Teleflex Medical

Recalled Item: RUSCH Foley Urinary Catheter Insertion Tray with 10cc syringe Recalled by...

The Issue: Labeling error: The manufacturing date is the same as the expiration date....

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

Class III — Low RiskOngoing
Medical DeviceJuly 9, 2014· Nanosphere, Inc.

Recalled Item: Verigene BC-GN Test Kit (Catalog number 20-005-021) includes: 1) 20 Recalled...

The Issue: Nanosphere Inc. has recently determined through four customer complaints...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2014· Carestream Health, Inc.

Recalled Item: Kodak DirectView DR 7500 Diagnostic X-Ray System Product Usage: The Recalled...

The Issue: An on-site evaluation of the equipment parts that attach the Beta Assembly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2014· Richard Wolf Medical Instruments Corp.

Recalled Item: The Hulka Clip is a sterile packaged medical device that Recalled by Richard...

The Issue: Richard Wolf Medical Instrument Corporation is recalling Hulka Clip Tubal...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2014· Gyrus Medical, Inc

Recalled Item: Gyrus ACMI Falope-Ring Dilator Recalled by Gyrus Medical, Inc Due to...

The Issue: Falope-Ring Dilator for Reusable Falope-Ring Band Applicators have been sold...

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

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

Recalled Item: Siemens Luminos dRF Recalled by Siemens Medical Solutions USA, Inc Due to It...

The Issue: It was discovered that during a RAD examination using Siemens Luminos dRF,...

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 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 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
Medical DeviceJuly 4, 2014· Advandx Inc

Recalled Item: AdvanDx Quick FISH Fixation Kit for BC ( Blood Cultures) Recalled by Advandx...

The Issue: Positive result in the Internal negative control well for the Staphylococcus...

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

Class II — Potential Health HazardOngoing
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· 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 with Catheter and Accessories 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 with SIPHONGUARD¿ Device Recalled by Codman &...

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
Medical DeviceJuly 3, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas - In line Valve with Unitized BACTISEAL¿ Catheter and...

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