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. 2,491 recalls have been distributed to Indiana in the last 12 months.
Showing 881–900 of 53,528 recalls
Recalled Item: Dynagel Recalled by Blossom Pharmaceuticals Due to cGMP deviations
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX800. Product Number: 865240. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phytonadione Injectable Emulsion Recalled by Cipla Limited Due to Failed...
The Issue: Failed Stability Specifications: Observed OOS results: eg results for colour...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX700. Product Number: 865241. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Arise 1000EX mattress Recalled by Stryker Medical Division of...
The Issue: Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MP90. Product Number: M8010A. Recalled by Philips North America...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX400. Product Number: 866060. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker MV3 bariatric bed Recalled by Stryker Medical Division of Stryker...
The Issue: Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Globe Zinc Oxide Ointment USP Zinc Oxide 20% Skin Protectant Recalled by...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine HCI 2% and Epinephrine 1:100 Recalled by Novocol Pharmaceutical of...
The Issue: Defective container: cracked/broken cartridges
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wecare Calasoothe Recalled by Blossom Pharmaceuticals Due to cGMP deviations
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX600. Product Number: 865242. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX500. Product Number: 866064. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX850. Product Number: 866470. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3% Polocaine DENTAL Recalled by Novocol Pharmaceutical of Canada, Inc. Due...
The Issue: Defective container: cracked/broken cartridges
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wecare Enema Recalled by Blossom Pharmaceuticals Due to cGMP deviations
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mai California Roll WR - .9 oz (167g) Recalled by HANA GROUP Due to Wheat...
The Issue: Wheat and Soy missing allergens from the product Contains Statement.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: IntelliVue MP5. Product Number: M8105A. Recalled by Philips North America...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Multi-Measurement Module X3. Product Number: 867030. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blonde Beard's Dojo Asian Wing Sauce Recalled by Blonde Beard's Due to...
The Issue: Undeclared Soy
Recommended Action: Do not consume. Return to store for a refund or discard.