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. 1,806 recalls have been distributed to Idaho in the last 12 months.
Showing 31041–31060 of 48,215 recalls
Recalled Item: 4C All Natural 100% Imported Italian Pecorino Romano Cheese Recalled by 4 C...
The Issue: FDA sample revealed the presence of Salmonella contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cento Parmesan Grated Cheese Recalled by 4 C Foods, Corp. Due to Potential...
The Issue: FDA sample revealed the presence of Salmonella contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 4C Homestyle All Natural 100% Imported Italian Pecorino Romano Cheese...
The Issue: FDA sample revealed the presence of Salmonella contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cento Romano Grated Cheese Recalled by 4 C Foods, Corp. Due to Potential...
The Issue: FDA sample revealed the presence of Salmonella contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Modular Necks: 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: Modular REDAPT(TM) Hip Systems The Modular SMF(TM) and Modular REDAPT(TM)...
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: 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: SOMATOM Definition AS System Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Software update that provides software and firmware bug-fixes to improve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge System Recalled by Siemens Medical Solutions USA,...
The Issue: Software update that provides software and firmware bug-fixes to improve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Flash System Recalled by Siemens Medical Solutions USA,...
The Issue: Software update that provides software and firmware bug-fixes to improve...
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: Desoximetasone Ointment USP Recalled by Akorn Inc Due to Failed Stability...
The Issue: Failed Stability Specifications; out-of specification value for homogeneity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ultimate Body Tox PRO capsules Recalled by Ultimate Body Tox Due to...
The Issue: Marketed Without An Approved NDA/ANDA: The product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Weight Watchers Smart Ones Recalled by KRAFT HEINZ FOODS COMPANY Due to...
The Issue: Possible contamination of product with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
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: 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: Lactulose Solution Recalled by VistaPharm, Inc. Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Products: bulk solution tested...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: L-Cysteine Hydrochloride Injection Recalled by Sandoz Inc Due to Lack of...
The Issue: Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: L-Cysteine Hydrochloride Injection Recalled by Sandoz Inc Due to Lack of...
The Issue: Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.