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. 2,768 recalls have been distributed to Indiana in the last 12 months.
Showing 3101–3120 of 53,528 recalls
Recalled Item: BD Care Coordination Engine (CCE) Infusion Adapter Recalled by CareFusion...
The Issue: Software issue that may result in outdated automated programming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CURAD Alcohol Prep Pads Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Alcohol Prep Pads Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ergocalciferol - Vitamin D Supplement - 10 mcg (400 Units) Recalled by...
The Issue: Defective Delivery System: Leakage observed after oral solution was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lorazepam 0.5 mg per 0.25 mL Oral Syringe Recalled by Safecor Health, LLC...
The Issue: Defective Delivery System: Leakage observed after oral solution was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ferrous Sulfate 7.5 mg Iron/0.5 mL Oral Syringe Recalled by Safecor Health,...
The Issue: Defective Delivery System: Leakage observed after oral solution was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morphine Sulfate 5 mg per 0.25 mL Oral Syringe Recalled by Safecor Health,...
The Issue: Defective Delivery System: Leakage observed after oral solution was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Simethicone 20 mg per 0.3 mL Oral Syringe Recalled by Safecor Health, LLC...
The Issue: Defective Delivery System: Leakage observed after oral solution was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Initiation 18 Coated Regular and 18 Coated Super Tampons Recalled by DAYE...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Initiation 18 Coated Regular and 18 Nude Regular Tampons Recalled by DAYE...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 18 Coated Regular and 18 Nude Regular Tampons Recalled by DAYE (ANNE'S DAY...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3 Month All in One Bundle Recalled by DAYE (ANNE'S DAY LTD) Due to Product...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9 Coated Super Tampons and 9 Nude Super Tampons Recalled by DAYE (ANNE'S DAY...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3 Month Regular Flow Bundle Recalled by DAYE (ANNE'S DAY LTD) Due to Product...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 18 Coated Regular Tampons Recalled by DAYE (ANNE'S DAY LTD) Due to Product...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Initiation 36 Coated Regular Tampons Recalled by DAYE (ANNE'S DAY LTD) Due...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9 Coated Super and 9 Nude Super Tampons Recalled by DAYE (ANNE'S DAY LTD)...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Initiation 3 Month Trial Tampon Box Recalled by DAYE (ANNE'S DAY LTD) Due to...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Initiation 3 Month All in One Bundle Recalled by DAYE (ANNE'S DAY LTD) Due...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Initiation 36 Coated Super Tampons Recalled by DAYE (ANNE'S DAY LTD) Due to...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.