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. 2,395 recalls have been distributed to Idaho in the last 12 months.
Showing 26741–26760 of 27,833 recalls
Recalled Item: Terumo Advanced Perfusion System 1 ASSEMBLY FLOW POD Product Usage: Recalled...
The Issue: Terumo Cardiovascular Systems (CVS) received two reports of the false back...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solara 3G Custom Manual Wheelchair Product Usage: To provide mobility...
The Issue: The potential exists for the wheel to rotate freely despite engagement of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Titanium Minimally Invasive Reduction Screw System Polyaxial Screw...
The Issue: This action is being initiated following a detailed investigation in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrumentation Industries BE183-SU and BE 183 SU-12 Manual Jet Ventilators...
The Issue: Firm initiated an update to Directions for Use necessitating replacement of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Titanium Minimally Invasive Reduction Screw System Locking Cap...
The Issue: This action is being initiated following a detailed investigation in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Clearlink System Buretrol Solution Set Recalled by Baxter Healthcare...
The Issue: Baxter has determined that the ball-valve feature of the Buretrol Solution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Clearlink System Buretrol Solution Set Recalled by Baxter Healthcare...
The Issue: Baxter has determined that the ball-valve feature of the Buretrol Solution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Interlink System Buretrol Solution Set with 150 mL Burette Recalled...
The Issue: Baxter has determined that the ball-valve feature of the Buretrol Solution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8 Fr. Bardex Pediatric All-Silicone Foley Catheter with a 3cc Recalled by...
The Issue: The 8 Fr. Bardex All-Silicone Foley Catheter with 3cc balloon had an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cemented Tibial Drill Product Usage: The cemented tibial drill is Recalled...
The Issue: Zimmer is initiating a recall of the Cemented Tibial Drill for the Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: materials "RETINAL OCT Analysis and Interpretation Method" shipped with...
The Issue: Devices labeled for an intended use not included in the existing 510(k) or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Interlink System Buretrol Solution Set Recalled by Baxter Healthcare...
The Issue: Baxter has determined that the ball-valve feature of the Buretrol Solution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 5.0 w/Needles with violet and blue Orthocord Product Number:...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 6.5 w/Needles with Orthocord Product Number: 222970 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 6.5 w/out Needles with Orthocord Product Number: 222971 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 5.0mm with Ethibond without needles Product Number: 222964 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 6.5 w/Needles with violet and blue Orthocord Product Number:...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 5.0 w/out Needles with violet and blue Orthocord Product Recalled...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 6.5mm with Ethibond without needles Product Number: 222966 SPIRALOK...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpiraLok 6.5 w/out Needles with violet and blue Orthocord Product Recalled...
The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.