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.

53,528 total recalls
2,592 in last 12 months

Showing 2040120420 of 53,528 recalls

Medical DeviceDecember 23, 2019· GE Healthcare, LLC

Recalled Item: SIGNA Architect Nuclear Magnetic Resonance Imaging System - Product Usage:...

The Issue: It was identified that due to a potential installation workflow issue, the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· Nikon Metrology

Recalled Item: Nikon Metrology XTH cabinet x-ray Systems which includes variations STH225...

The Issue: The manufacturer identified a risk that their products might fail to comply...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· GE Healthcare, LLC

Recalled Item: SIGNA Vibrant Nuclear Magnetic Resonance Imaging System Recalled by GE...

The Issue: It was identified that due to a potential installation workflow issue, the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· GE Healthcare, LLC

Recalled Item: SIGNA Premier Nuclear Magnetic Resonance Imaging System - Product Usage:...

The Issue: It was identified that due to a potential installation workflow issue, the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· GE Healthcare, LLC

Recalled Item: SIGNA Pioneer Nuclear Magnetic Resonance Imaging System - Product Usage:...

The Issue: It was identified that due to a potential installation workflow issue, the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· Carroll-Baccari, Inc.

Recalled Item: LemonPrep Tubes (MD0019-T) and Single use cups (MD0019-SUP) Recalled by...

The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· Carroll-Baccari, Inc.

Recalled Item: MVAP MEDICAL SUPPLIES INC Recalled by Carroll-Baccari, Inc. Due to Samples...

The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· Carroll-Baccari, Inc.

Recalled Item: PediaPrep Tubes (MD0033-T) and Single use cups (MD0033-SUP) Recalled by...

The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· Zimmer Biomet, Inc.

Recalled Item: Jamshidi Bone Marrow Aspiration Needle Item Number: 00-1103-007-00 Recalled...

The Issue: Potential for the expiration date on the outer label that was applied by...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· Carroll-Baccari, Inc.

Recalled Item: Wave Prep Tubes (1710-03) and single use cups (17--00-24) Recalled by...

The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· Philips North America, LLC

Recalled Item: VesselNavigator application used with Philips Azurion (Azurion 7 Series)...

The Issue: Due to a software defect, when a digital subtraction angiography (DSA) is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugDecember 23, 2019· GSK Consumer Health, Inc

Recalled Item: Theraflu Cough Relief Recalled by GSK Consumer Health, Inc Due to Labeling:...

The Issue: Labeling: Label Lacks Warning: Product recalled due to absence of a warning...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2019· Assurance Infusion

Recalled Item: CLON 500MCG/HYDROM 5MG/ML INJ in 20 mL syringe Assurance Infusion Recalled...

The Issue: Lack of sterility assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2019· Assurance Infusion

Recalled Item: MORPHINE 10MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800...

The Issue: Lack of sterility assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2019· Assurance Infusion

Recalled Item: Alprostadil 40 mcg/mL (2 mL vial) Inj. Soln. in 2 Recalled by Assurance...

The Issue: Lack of sterility assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2019· Assurance Infusion

Recalled Item: BUP 10MG/HYDROM 10MG/MORP 2MG/SUF 250MCG/ML INJ in 20 mL syringe Recalled by...

The Issue: Lack of sterility assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2019· Assurance Infusion

Recalled Item: QUADMIX 30MG/2MG/20MCG/100MCG/ML INJ in 1 mL vial Assurance Infusion (713)...

The Issue: Lack of sterility assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2019· Assurance Infusion

Recalled Item: FENTANYL 3000MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800...

The Issue: Lack of sterility assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2019· Assurance Infusion

Recalled Item: BAC 400MCG/BUP 20MG/HYDROM 15MG/SUF 1000MCG/ML INJ in 20 mL syringe Recalled...

The Issue: Lack of sterility assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2019· Assurance Infusion

Recalled Item: HCG 1 Recalled by Assurance Infusion Due to Lack of sterility assurance.

The Issue: Lack of sterility assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund