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. 1,003 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
1,003 in last 12 months

Showing 20281–20300 of 48,215 recalls

Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: SM DIS VOL/DORS RAD LAT COL PLATE Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Zimmer Biomet, Inc.

Recalled Item: Coorad Morrey Total Elbow Recalled by Zimmer Biomet, Inc. Due to Non-highly...

The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2019· Hologic, Inc

Recalled Item: Panther Fusion Extraction Reagent-S Recalled by Hologic, Inc Due to Reagent...

The Issue: Reagent component included in flu test kit may cause both high background...

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

Class II — Potential Health HazardOngoing
DrugOctober 10, 2019· Innoveix Pharmaceuticals Inc

Recalled Item: Lyophilized Human Chorionic Gonadotropin 5 Recalled by Innoveix...

The Issue: Lack of Sterility Assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2019· Innoveix Pharmaceuticals Inc

Recalled Item: Lyophilized Chorionic Gonadotropin 11 Recalled by Innoveix Pharmaceuticals...

The Issue: Lack of Sterility Assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2019· Innoveix Pharmaceuticals Inc

Recalled Item: Lyophilized Sermorelin w/ GHRP2 3 mg For injection Recalled by Innoveix...

The Issue: Lack of Sterility Assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2019· Innoveix Pharmaceuticals Inc

Recalled Item: Lyophilized Human Chorionic Gonadotropin 5 Recalled by Innoveix...

The Issue: Lack of Sterility Assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2019· Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Recalled Item: PF-Fentanyl Citrate 2 mcg/mL* & Bupivacaine HCl 0.125% in 0.9% Recalled by...

The Issue: GMP Deviations: potential glass contamination

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2019· Ingenus Pharmaceuticals Llc

Recalled Item: Leucovorin Calcium Injection Recalled by Ingenus Pharmaceuticals Llc Due to...

The Issue: Crystallization: Presence of particulate matter identified as API...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2019· Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Recalled Item: PF-Fentanyl Citrate (2 mcg/mL)* & Bupivacaine HCl 0.0625 in 0.9% Recalled by...

The Issue: GMP Deviations: potential glass contamination

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2019· Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Recalled Item: Amino Acid Injection 50 g/1000 mL (50 mg/mL) 25 g L-Arginine HCl Recalled by...

The Issue: Lack of Assurance of Sterility; bags have potential to leak

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2019· Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Recalled Item: PF-Fentanyl Citrate 2 mcg/mL* & Ropivacaine HCl 0.1% in 0.9% Recalled by...

The Issue: GMP Deviations: potential glass contamination

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2019· Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Recalled Item: del Nido Cardioplegia Solution Recalled by Nephron Pharmaceuticals...

The Issue: Lack of Assurance of Sterility; bags have potential to leak

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 9, 2019· Medivators, Inc.

Recalled Item: Medivators Endo Smartcap Endoscope Tubing. Recalled by Medivators, Inc. Due...

The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Medivators, Inc.

Recalled Item: Medivators EndoGator . Kit for Olympus 140/160/180/190 Series GI Recalled by...

The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Stryker Sustainability Solutions

Recalled Item: Zimmer Tourniquet Cuff 30" (Blue) Recalled by Stryker Sustainability...

The Issue: Tourniquet cuffs are potentially mislabeled. If used may lead to (1) Device...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Medivators, Inc.

Recalled Item: Medivators Endo Smartcap Endoscope Tubing. . Packaged as Contents 1 Recalled...

The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Medivators, Inc.

Recalled Item: Medivators EndoGator . Kit for Olympus 140/160/180/190 Series GI Recalled by...

The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Medivators, Inc.

Recalled Item: Medivators Endo carry-on Procedure Kit - Product Usage: Recalled by...

The Issue: Medivators is recalling Endo SmartCap Tubing due to a manufacturing anomaly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2019· Nextremity Solutions

Recalled Item: Stratum Foot Plating System-NL LP Screw 3.5x50mm ST Recalled by Nextremity...

The Issue: Product labeled as STRM-NL-3550ST, NL LP Screw 3.5x50mm ST, lot M1151 may...

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

Class II — Potential Health HazardOngoing