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. 2,768 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,768 in last 12 months

Showing 20212040 of 53,528 recalls

DrugJuly 9, 2025· Boothwyn Pharmacy LLC

Recalled Item: Semaglutide Recalled by Boothwyn Pharmacy LLC Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 9, 2025· Boothwyn Pharmacy LLC

Recalled Item: Semaglutide Recalled by Boothwyn Pharmacy LLC Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 9, 2025· Strides Pharma, Inc.

Recalled Item: Cinacalcet Tablets 90 mg Recalled by Strides Pharma, Inc. Due to Failed...

The Issue: Failed Dissolution Specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 9, 2025· Imprimis NJOF, LLC

Recalled Item: Tropicamide-Proparacaine-Phenylephrine-Ketorolac Recalled by Imprimis NJOF,...

The Issue: Sub-Potent Drug: Subpotent assay results during stability testing.

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

Class III — Low RiskOngoing
Refund
DrugJuly 9, 2025· Imprimis NJOF, LLC

Recalled Item: Epinephrine Lidocaine HCL Recalled by Imprimis NJOF, LLC Due to Sub-Potent...

The Issue: Sub-Potent Drug: Subpotent assay results during stability testing.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 9, 2025· Ascend Laboratories, LLC

Recalled Item: Rizatriptan Benzoate Tablets Recalled by Ascend Laboratories, LLC Due to...

The Issue: CGMP Deviations: detection of N-nitroso-dimethyl-rizatriptan impurity, above...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 9, 2025· Ascend Laboratories, LLC

Recalled Item: Rizatriptan Benzoate Tablets Recalled by Ascend Laboratories, LLC Due to...

The Issue: CGMP Deviations: detection of N-nitroso-dimethyl-rizatriptan impurity, above...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 9, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products Ca Slides Recalled by Ortho-Clinical Diagnostics,...

The Issue: Generations 67 and above of VITROS Ca Slides are experiencing an increased...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2025· Encore Medical, LP

Recalled Item: Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Recalled by Encore...

The Issue: Knee implants contain incorrect labeling (size and/or side incorrect)

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2025· Encore Medical, LP

Recalled Item: Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Recalled by Encore...

The Issue: Knee implants contain incorrect labeling (size and/or side incorrect)

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2025· Ambu Inc.

Recalled Item: Ambu SPUR II Labeled as the following: 1 SPUR II Adult Resuscitator Recalled...

The Issue: Potential for the manometer port being blocked rendering the manometer...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 9, 2025· B BRAUN MEDICAL INC

Recalled Item: Microbore Extension Set with 0.2 Micron Filter. Catalog Number: V6215....

The Issue: Label is incorrect. The product label indicates that the device contains an...

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

Class I — Serious Health HazardOngoing
FoodJuly 8, 2025· SHEEHAN BROTHERS VENDING

Recalled Item: Sheehan Brothers Vending Cheeseburger Recalled by SHEEHAN BROTHERS VENDING...

The Issue: Undeclared sesame

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 8, 2025· SHEEHAN BROTHERS VENDING

Recalled Item: Sheehan Brothers Vending Pepperoni Pizza Mini Sub Recalled by SHEEHAN...

The Issue: Undeclared sesame

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 8, 2025· SHEEHAN BROTHERS VENDING

Recalled Item: Sheehan Brothers Vending Italian Mini Sub Recalled by SHEEHAN BROTHERS...

The Issue: Undeclared sesame

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 8, 2025· SHEEHAN BROTHERS VENDING

Recalled Item: Sheehan Brothers Vending Spicy Chicken Sandwich Recalled by SHEEHAN BROTHERS...

The Issue: Undeclared sesame

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 8, 2025· SHEEHAN BROTHERS VENDING

Recalled Item: Sheehan Brothers Vending BBQ Riblet Sandwich with Coleslaw Recalled by...

The Issue: Undeclared sesame

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 8, 2025· SHEEHAN BROTHERS VENDING

Recalled Item: Sheehan Brothers Vending Chili Cheese Coney Recalled by SHEEHAN BROTHERS...

The Issue: Undeclared sesame

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 8, 2025· Mondelez Global Llc

Recalled Item: Ritz Peanut Butter Cracker Sandwiches Recalled by Mondelez Global Llc Due to...

The Issue: Undeclared allergens (Peanut) due to mispackaging

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 8, 2025· Mondelez Global Llc

Recalled Item: Ritz Peanut Butter Cracker Sandwiches Recalled by Mondelez Global Llc Due to...

The Issue: Undeclared allergens (Peanut) due to mispackaging

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

Class II — Potential Health HazardOngoing
Refund