Product Recalls in Indiana
Product recalls affecting Indiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Indiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,592 recalls have been distributed to Indiana in the last 12 months.
Showing 19901–19920 of 53,528 recalls
Recalled Item: Captus 4000e Thyroid Uptake System Recalled by Capintec Inc Due to It is...
The Issue: It is possible that the collimators have screw hole locations that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinix-8000C with Catheterization Table CAT-850B or CAT-860B - Product...
The Issue: Bolts holding the longitudinal movement of catheterization tables may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinix-8000F with Catheterization Table CAT-850B or CAT-860B - Product...
The Issue: Bolts holding the longitudinal movement of catheterization tables may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merits E604 Pilot Navigator Stairlift - Product Usage: To transport Recalled...
The Issue: Pinion gear may disengage from track allowing lift to slip or jolt.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens N Latex CDT Kit- IVD quantitative determination of...
The Issue: Negative bias for the carbohydrate-deficient transferrin (CDT) measurement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) patches Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for mechanical peel and shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) patches Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for mechanical peel and shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carbidopa and Levodopa Tablets Recalled by Mayne Pharma Inc Due to Product...
The Issue: Product Mix-Up: A foreign tablet was found in bottle.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) patches Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for mechanical peel and shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) patches Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for mechanical peel and shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ReStructure VANILLA PROTEIN POWDER NET WT. 527G POUCH & 27G Recalled by New...
The Issue: The firm was notified that the labeling does not include the word milk on...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Merlin PCS 3650 Software Upgrade Kit Recalled by Abbott Due to Internal...
The Issue: Internal testing of software identified software anomaly scenarios where if...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Lumbar Puncture Tray. Anesthesia Conduction Kit. 4826PL-20 - Product...
The Issue: Cases of Portex¿ Lumbar Puncture Tray Child, SKU #4826PL-20 had been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ReWalk Personal 6.0 Recalled by Argo Medical Technologies Ltd Due to ReWalk...
The Issue: ReWalk Robotics received two complaints (one in the US; one in the Germany),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAVIO Soft Tissue Protector Recalled by Smith & Nephew, Inc. Due to...
The Issue: Potential for the NAVIO Soft Tissue Protector to become stuck or bound to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH 930 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Editing an assay Test Definition and switching to another assay s Test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Hydrogel Ag 4x4 Recalled by Gentell, Inc Due to During an FDA audit,...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Hydrogel Ag 4oz. Tube Recalled by Gentell, Inc Due to During an FDA...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Hydrogel Ag 2x2 Recalled by Gentell, Inc Due to During an FDA audit,...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Hydrogel Ag 4x8 Recalled by Gentell, Inc Due to During an FDA audit,...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.