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. 2,447 recalls have been distributed to Idaho in the last 12 months.
Showing 18641–18660 of 27,833 recalls
Recalled Item: Reunion TSA Peg Alignment Sound Catalog #5901-1038 The Peg Alignment...
The Issue: Reunion TSA Peg Alignment Sound broke during surgery.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Special Connector Instruments (Special Connector Recalled by K2M, Inc...
The Issue: Instruments were developed without adequate consideration given to the need...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRU-Balance 3 Power Positioning Systems Recalled by Pride Mobility Products...
The Issue: The interface between the TB3 back and tilt base can separate when tilted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PreludeEASE Hydrophilic Sheath Introducer Dilator The Merit PreludeEASE...
The Issue: Recalling dilators included with the 6F PreludeEASE Hydrophilic Sheath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8450-010-040 4.0MM Round Recalled by Stryker Instruments Div. of Stryker...
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8470-009-030 3.0MM Precision Round Recalled by Stryker Instruments Div. of...
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8450-009-030 3.0MM Precision Round Recalled by Stryker Instruments Div. of...
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8450-107-525 2.5MM Precision Match Head Recalled by Stryker Instruments Div....
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8450-009-040 4.0MM Precision Round Recalled by Stryker Instruments Div. of...
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AtriClip" LAA Exclusion System with preloaded Gillinov-Cosgrove" Clip - A...
The Issue: A complaint of the PRO2 jaw breaking prior to surgery being performed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8470-009-040 4.0MM Precision Round Recalled by Stryker Instruments Div. of...
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8450-107-530 3.0MM Precision Match Head Recalled by Stryker Instruments Div....
The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical Oasis Pediatric Drain as follows: 3612-100 Oasis...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical Pediatric Chamber Ocean Drains as follows: 2012-320 Ocean...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical Ocean Drains as follows: 2002-000 Ocean single drain Recalled...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes VA Implant Rack for the Compact Distal Radius System Recalled by...
The Issue: The screw rack plate was assembled incorrectly which could cause the screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical 16400 Express Mini 500 dry seal drain Product Recalled by...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical 3620-100: Oasis dual chamber drain with in-line connectors...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sekisui Diagnostics Ammonia L3K¿ Assay Recalled by Sekisui Diagnostics...
The Issue: Certain lots are showing an atypical decrease in optical density (OD) over...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Medical Oasis Blood Recovery Drains as follows: 3650-100 Oasis...
The Issue: Outer Packaging is not sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.