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 18721–18740 of 27,833 recalls
Recalled Item: Modular SMF(TM) The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems...
The Issue: All lots of modular neck hip prostheses are being recalled due to a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Empowr Knee System Product Usage: Non-porous proximal tibial baseplate...
The Issue: A size 4 Empowr baseplate was mislabeled as a size 6. The affected lot was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Recalled by Smith & Nephew, Inc. Due to Lack of 510k...
The Issue: Lack of 510k clearance for design modification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed...
The Issue: An increase in reports indicating that the reprocessed H12LP Trocar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Recalled by Smith & Nephew, Inc. Due to Lack of 510k...
The Issue: Lack of 510k clearance for design modification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard C-Section Drape with Clear Screen and Full Incise (Non-Sterile)...
The Issue: Drapes within the affected lots may include a manufacturing variation that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 4.0 Recalled by RAYSEARCH LABORATORIES AB Due to Software...
The Issue: Software anomaly; an issue was found with the proton Pencil Beam Scanning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Virtual XD Light Body Regular Set Wash Material Recalled by Ivoclar...
The Issue: The firm received complaints claiming the dental material failed to set up....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Virtual XD Light Body Fast Set Wash Material Recalled by Ivoclar Vivadent,...
The Issue: The firm received complaints claiming the dental material failed to set up....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Virtual XD Test Pack Heavy/Light Fast Set Recalled by Ivoclar Vivadent, Inc....
The Issue: The firm received complaints claiming the dental material failed to set up....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GAM Kirschner Wire Recalled by Stryker Howmedica Osteonics Corp. Due to A...
The Issue: A review of packaging revealed the seal integrity of the pouch may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW OnControl Bone Marrow Biopsy System Comprehensive Tray Recalled by...
The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW OnControl Bone Marrow Biopsy System Tray Recalled by Teleflex Medical...
The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREMIER EHEC and PREMIER EHEC Bulk. Recalled by Meridian Bioscience Inc Due...
The Issue: Internal testing has demonstrated that the indicated kit lots produce false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW OnControl Bone Lesion Biopsy System Tray Recalled by Teleflex Medical...
The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OnControl Biopsy System Ported Needle Tray Recalled by Teleflex Medical Due...
The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Performance-LOAD Ambulance Cot Fastener Stretcher Recalled by Stryker...
The Issue: Stryker Medical initiated a voluntary recall of Stryker Performance-LOAD Cot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW OnControl Ported Aspiration System Tray Recalled by Teleflex Medical...
The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Spinal Anesthesia Tray The BD Spinal Anesthesia Tray is Recalled by...
The Issue: BD is conducting a voluntary product recall of the BD Spinal Anesthesia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDRAD Intego PET Infusion System - Pump Intended to deliver Recalled by...
The Issue: Bayer has determined that all current Source Administration Sets (SAS) used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.