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. 2,723 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,723 in last 12 months

Showing 1046110480 of 53,528 recalls

DrugJanuary 11, 2023· Amerisource Health Services LLC

Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Amerisource Health...

The Issue: Failed Dissolution Specifications: This recall is being initiated in support...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2023· Consolidated Chemical, Inc

Recalled Item: Humatrix Microclysmic Gel Recalled by Consolidated Chemical, Inc Due to CGMP...

The Issue: CGMP Deviations: initiated due to violations of CGMP manufacturing practices

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2023· Consolidated Chemical, Inc

Recalled Item: Techni-Care Chloroxylenold 3% Recalled by Consolidated Chemical, Inc Due to...

The Issue: CGMP Deviations: initiated due to violations of CGMP manufacturing practices

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 10, 2023· Superior Fresh, LLC

Recalled Item: Superior Crunch Net Wt. 4 oz. (113g). Ingredients May Contain Green Leaf...

The Issue: Foreign material (small glass particles)

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 10, 2023· Superior Fresh, LLC

Recalled Item: Superior Fresh Lettuce Blend Ingredients May Contain Red Leaf Recalled by...

The Issue: Foreign material (small glass particles)

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 10, 2023· Superior Fresh, LLC

Recalled Item: Superior Fresh Lettuce Blend Ingredients May Contain Red Leaf Recalled by...

The Issue: Foreign material (small glass particles)

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 10, 2023· Superior Fresh, LLC

Recalled Item: Superior Fresh Organic Spring Mix Family Pack. Recalled by Superior Fresh,...

The Issue: Foreign material (small glass particles)

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 10, 2023· Superior Fresh, LLC

Recalled Item: Superior Fresh Mighty Mix Recalled by Superior Fresh, LLC Due to Foreign...

The Issue: Foreign material (small glass particles)

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 10, 2023· Superior Fresh, LLC

Recalled Item: Superior Fresh Organic Raw Spring Mix. 1 lb. Bag Recalled by Superior Fresh,...

The Issue: Foreign material (small glass particles)

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Folate 140 test kit- For in vitro diagnostic Recalled by Siemens...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Folate 700 test kit (REF)-For in vitro diagnostic Recalled by...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur Folate 100 test kit-For in vitro diagnostic use Recalled by...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Folate 700 test kit- For in vitro diagnostic Recalled by Siemens...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur Folate 500 test kit (REF)-For in vitro diagnostic Recalled by...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur Folate 500 test kit- For in vitro diagnostic Recalled by...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
DrugJanuary 6, 2023· Nephron Sterile Compounding Center LLC

Recalled Item: Rocuronium Bromide Injection Recalled by Nephron Sterile Compounding Center...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 5, 2023· Ascend Laboratories, LLC

Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Ascend...

The Issue: Failed Dissolution Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 5, 2023· Ascend Laboratories, LLC

Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Ascend...

The Issue: Failed Dissolution Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 5, 2023· Ascend Laboratories, LLC

Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Ascend...

The Issue: Failed Dissolution Specification

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 5, 2023· MACLEODS PHARMA USA, INC

Recalled Item: Levofloxacin Tablets Recalled by MACLEODS PHARMA USA, INC Due to Mismatching...

The Issue: Mismatching of the embossing on the tablets (T7) with the embossing...

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

Class III — Low RiskOngoing
Refund