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. 1,783 recalls have been distributed to Idaho in the last 12 months.
Showing 32661–32680 of 48,215 recalls
Recalled Item: Zenostar MT Color A3.5 60ml Recalled by Ivoclar Vivadent, Inc. Due to The...
The Issue: The primary packaging of these products may show leaks in individual cases....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novation Press-Fit Splined RDD Recalled by Exactech, Inc. Due to Labeled...
The Issue: Labeled with the incorrect Global Trade Item Number (GTIN). The GTIN on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The surface inside of the femoral component, where cement is applied for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONLINE TDM Vancomycin 100 tests Recalled by Roche Diagnostics Operations,...
The Issue: Roche Diagnostics Operations, Inc. has issued a voluntary recall for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA¿ Centaur XPT system software versions V1.0.1 (Bundle 1.0.912 SMN...
The Issue: Eight (8) issues were identified which may affect the results generated by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The surface inside of the femoral component, where cement is applied for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The surface inside of the femoral component, where cement is applied for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The surface inside of the femoral component, where cement is applied for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The surface inside of the femoral component, where cement is applied for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The surface inside of the femoral component, where cement is applied for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novation Press-Fit Splined RDD Recalled by Exactech, Inc. Due to Labeled...
The Issue: Labeled with the incorrect Global Trade Item Number (GTIN). The GTIN on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remeven Cream Recalled by Stratus Pharmaceuticals Inc Due to...
The Issue: Crystallization; Complaints that cream appears to have crystallized
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kamedis BIO-HERBAL DANDRUFF CARE THERAPEUTIC 2-STEP DANDRUFF CARE SYSTEM -...
The Issue: Subpotent Drug: Out of Specification assay values on stability for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril Tablets USP Recalled by Sandoz Inc Due to Labeling: Incorrect or...
The Issue: Labeling: Incorrect or Missing Package Insert
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: iConnect Access software. The firm name on the label is Merge Healthcare...
The Issue: Software displayed incorrect prior reports in the viewport area, only when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT Model 882482 Recalled by Philips Medical Systems (Cleveland)...
The Issue: The firm became aware of an issue where during a non-Auto Body Contouring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT Upgrade Model 882454 Recalled by Philips Medical Systems...
The Issue: The firm became aware of an issue where during a non-Auto Body Contouring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X Recalled by Philips Medical Systems (Cleveland) Inc Due to The...
The Issue: The firm became aware of an issue where during a non-Auto Body Contouring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK CR Plus and/or LIFEPAK EXPRESS are Automatic External...
The Issue: LIFEPAK CR Plus Automated External Defibrillators (AED) or LIFEPAK EXPRESS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OUTBACK STEAKHOUSE OSI Mama's Batter Recalled by Magic Seasoning Blends, LLC...
The Issue: There is a potential presence of peanut protein in certain lots of milled...
Recommended Action: Do not consume. Return to store for a refund or discard.