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. 2,547 recalls have been distributed to Indiana in the last 12 months.
Showing 27481–27500 of 53,528 recalls
Recalled Item: Driscoll's Blackberries Recalled by Driscoll's Strawberry Associates, Inc....
The Issue: Random sample indicated an over tolerance for three pesticides: Thidiazuron;...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Calendula Cream Recalled by Boiron Inc. Due to Labeling: Labeling Error on...
The Issue: Labeling: Labeling Error on Declared Strength; The outer carton (secondary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Merlin PCS Programmer software model 3330 Recalled by St Jude Medical,...
The Issue: Devices inappropriately displayed a low battery indicator determined to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Recalled by CareFusion 303, Inc. Due to The bezel manufacturing...
The Issue: The bezel manufacturing process for the FR-110 plastic may have resulted in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CSI Recalled by Cardiovascular Systems Inc Due to The pumps may switch to...
The Issue: The pumps may switch to stand-by during use requiring the pump to be reset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Infusion Pump Recalled by Smiths Medical ASD Inc. Due to...
The Issue: Certain Barrel Clamp Guides may contain a ridge that could potentially lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rhino 69 Extreme 50000 packaged in 1 capsule per blister pack Recalled by...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NEOstigmine Methylsulfate (1 mg/mL) 3mg per 3mL. 3mL Single Dose Recalled by...
The Issue: Lack of Assurance of Sterility:Microbial contamination was detected during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morphine Sulfate 2 mg/mL PF Injection. 1 mL in a Recalled by Premier...
The Issue: Lack of Assurance of Sterility:Microbial contamination was detected during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morphine Sulfate 4 mg/mL PF Injection. 1 mL in a Recalled by Premier...
The Issue: Lack of Assurance of Sterility:Microbial contamination was detected during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone HCl 1 mg/mL PF INJ. 1mL in a 3mL Recalled by Premier Pharmacy...
The Issue: Lack of Assurance of Sterility:Microbial contamination was detected during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sugarfina Platinum Bling Ring Recalled by Sugarfina, LLC Due to Internal...
The Issue: Internal audit discovered that their Platinum Bling Ring product contains...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cold Smoked Wild Coho Salmon Lox Recalled by Seabear Company Due to Mislabeling
The Issue: Products recalled due to water phase salt deviations and mislabeling of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hot Smoked Keta Beergarden Salmon Recalled by Seabear Company Due to Mislabeling
The Issue: Products recalled due to water phase salt deviations and mislabeling of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FlowGate2 Balloon Guide Catheter Recalled by Stryker Neurovascular Due to...
The Issue: There may be product manufactured with the outer diameter of the balloon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The BD Vacutainer Plus Plastic Citrate Blood Collection Tube is Recalled by...
The Issue: Approximately 3.4% of BD Vacutainer Plus Plastic Citrate Blood Collection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The BD Vacutainer Plus Plastic Citrate Blood Collection Tube is Recalled by...
The Issue: Approximately 3.4% of BD Vacutainer Plus Plastic Citrate Blood Collection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The BD Vacutainer Plus Plastic Citrate Blood Collection Tube is Recalled by...
The Issue: Approximately 3.4% of BD Vacutainer Plus Plastic Citrate Blood Collection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4Fr. Catheter Clamp with Fastener Recalled by Arrow International Inc Due to...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8Fr. Catheter Clamp with Fastener Recalled by Arrow International Inc Due to...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.