Product Recalls in Missouri

Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,060 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,060 in last 12 months

Showing 15441–15460 of 52,570 recalls

DrugJuly 27, 2021· Perrigo Company PLC

Recalled Item: GoodSense Aller.Ease 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: KIRKLAND ALLER-FEX 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: Rite Aid ALLERGY RELIEF Fexofenadine Hydrochloride tablets Recalled by...

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: Kroger 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: allergyrelief 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: 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: amazon basic+care 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: Rite Aid ALLERGY RELIEF Fexofenadine Hydrochloride tablets Recalled by...

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: Health Mart 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: basic+care 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 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· 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· 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
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 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· 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· 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· 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 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 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