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. 2,658 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,658 in last 12 months

Showing 1568115700 of 53,528 recalls

DrugJuly 27, 2021· Perrigo Company PLC

Recalled Item: Perrigo Fexofenadine Hydrochloride tablets Recalled by Perrigo Company PLC...

The Issue: Failed Impurities/Degradation Specifications; Out of specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2021· Perrigo Company PLC

Recalled Item: berkley jensen Recalled by Perrigo Company PLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications; Out of specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2021· Perrigo Company PLC

Recalled Item: CVS Allergy Relief Recalled by Perrigo Company PLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications; Out of specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2021· Perrigo Company PLC

Recalled Item: MAJOR Recalled by Perrigo Company PLC Due to Failed Impurities/Degradation...

The Issue: Failed Impurities/Degradation Specifications; Out of specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2021· High Performance Formulas, L.L.C. (HPF, L.L.C.)

Recalled Item: Cholestene capsules Recalled by High Performance Formulas, L.L.C. (HPF,...

The Issue: Marketed Without an Approved NDA/ANDA

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 26, 2021· Philips Respironics, Inc.

Recalled Item: Trilogy EV300 Recalled by Philips Respironics, Inc. Due to Two software...

The Issue: Two software issues have been identified related to pressure increase in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Philips Respironics, Inc.

Recalled Item: Trilogy Evo O2 Recalled by Philips Respironics, Inc. Due to Two software...

The Issue: Two software issues have been identified related to pressure increase in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Universal Recalled by Philips Respironics, Inc. Due to Two...

The Issue: Two software issues have been identified related to pressure increase in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Paltop Advanced Dental Solutions Ltd

Recalled Item: Scan Abutment PCA Recalled by Paltop Advanced Dental Solutions Ltd Due to...

The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Paltop Advanced Dental Solutions Ltd

Recalled Item: Scan Abutment SU Recalled by Paltop Advanced Dental Solutions Ltd Due to...

The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Paltop Advanced Dental Solutions Ltd

Recalled Item: Scan Abutment SP Recalled by Paltop Advanced Dental Solutions Ltd Due to...

The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Paltop Advanced Dental Solutions Ltd

Recalled Item: Scan Abutment MU Recalled by Paltop Advanced Dental Solutions Ltd Due to...

The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Two software issues...

The Issue: Two software issues have been identified related to pressure increase in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Paltop Advanced Dental Solutions Ltd

Recalled Item: Scan Abutment NP Recalled by Paltop Advanced Dental Solutions Ltd Due to...

The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Paltop Advanced Dental Solutions Ltd

Recalled Item: Scan Abutment WP Recalled by Paltop Advanced Dental Solutions Ltd Due to...

The Issue: Some devices are outside tolerances and showed a maximal deviation of 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2021· Abbott Laboratories

Recalled Item: Alinity ci-series System Control Module clinical chemistry and immunoassay...

The Issue: Due to potential performance issues with software version 3.2.3 and earlier....

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

Class II — Potential Health HazardOngoing
FoodJuly 26, 2021· CAHILLS FARM CHEESE LIMITED

Recalled Item: Lidl Preferred Selection-Irish Stout Cheddar - 7 oz. Recalled by CAHILLS...

The Issue: Cheese may be contaminated with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 26, 2021· CAHILLS FARM CHEESE LIMITED

Recalled Item: Lidl Preferred Selection-Red Wine Cheddar - 7 oz. Recalled by CAHILLS FARM...

The Issue: Cheese may be contaminated with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 26, 2021· CAHILLS FARM CHEESE LIMITED

Recalled Item: 1. Cahills Ireland Original Irish Porter 5lbs.Waxed Deli Wheel 2. Recalled...

The Issue: Cheese may be contaminated with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 26, 2021· CAHILLS FARM CHEESE LIMITED

Recalled Item: Cahills Ireland Red Wine - 5 lbs. Waxed Deli Wheel Recalled by CAHILLS FARM...

The Issue: Cheese may be contaminated with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund