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. 2,741 recalls have been distributed to Indiana in the last 12 months.
Showing 6121–6140 of 53,528 recalls
Recalled Item: Optum Nimbus II Plus Recalled by OptumHealth Care Solutions LLC Due to...
The Issue: Nimbus II Plus, Infusion Pump Systems, manufactured by InfuTronix, are being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pain Wizard Recalled by ARG Laboratories, Inc. Due to Out of Specification...
The Issue: Out of Specification for active ingredient. Violative grade of propylene...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pain Wizard Recalled by ARG Laboratories, Inc. Due to Out of Specification...
The Issue: Out of Specification for active ingredient. Violative grade of propylene...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NATURAL PAIN RELIEVING CREAM Recalled by ARG Laboratories, Inc. Due to Out...
The Issue: Out of Specification for active ingredient. Violative grade of propylene...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NATURAL PAIN RELIEVING CREAM Recalled by ARG Laboratories, Inc. Due to Out...
The Issue: Out of Specification for active ingredient. Violative grade of propylene...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NATURAL PAIN RELIEVING CREAM Recalled by ARG Laboratories, Inc. Due to Out...
The Issue: Out of Specification for active ingredient. Violative grade of propylene...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NATURAL PAIN RELIEVING CREAM Recalled by ARG Laboratories, Inc. Due to Out...
The Issue: Out of Specification for active ingredient. Violative grade of propylene...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pain Wizard Recalled by ARG Laboratories, Inc. Due to Out of Specification...
The Issue: Out of Specification for active ingredient. Violative grade of propylene...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ALOE GATOR Recalled by ARG Laboratories, Inc. Due to Out of Specification...
The Issue: Out of Specification for active ingredient
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ALOE GATOR Recalled by ARG Laboratories, Inc. Due to Out of Specification...
The Issue: Out of Specification for active ingredient
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pain Wizard Recalled by ARG Laboratories, Inc. Due to Out of Specification...
The Issue: Out of Specification for active ingredient. Violative grade of propylene...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bull Frog SPF 50 Amphibious Lotion SPF 50 Amphibious Lotion Recalled by ARG...
The Issue: Out of Specification for active ingredient
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Syringes labeled as: a) SYR 10ML L/L CONTROL Recalled by MEDLINE INDUSTRIES,...
The Issue: These syringes were identified to be affected by the FDA Safety Alert issued...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Pump Rotor Recalled by Fresenius Medical Care Holdings, Inc. Due to An...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra¿ Cranial access kit (without Prep solutions) Bit and Guard- Recalled...
The Issue: Potential holes and tears in the sterile packaging (header bag) of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T BlueStar Hemodialysis Machine Recalled by Fresenius Medical Care...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T BlueStar Hemodialysis Machine Recalled by Fresenius Medical Care...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T BlueStar Hemodialysis Machine Recalled by Fresenius Medical Care...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T BlueStar Hemodialysis Machine Recalled by Fresenius Medical Care...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.