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. 1,929 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
1,929 in last 12 months

Showing 2576125780 of 53,528 recalls

DrugAugust 2, 2018· Pharmcore Inc.

Recalled Item: Human Chorionic Gonadotropin 20000 IU Vial Lyophilized 1109 East Hallandale...

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
DrugAugust 2, 2018· Pharmcore Inc.

Recalled Item: Methylcobalamin 10 mg vial Lyophilized 1109 East Hallandale Beach Blvd....

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
DrugAugust 2, 2018· Pharmcore Inc.

Recalled Item: Human Chorionic Gonadotropin 5000 IU Vial Lyophilized 1109 East Hallandale...

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
DrugAugust 2, 2018· Pharmcore Inc.

Recalled Item: Human Chorionic Gonadotropin 6000 IU Vial Lyophilized 1109 East Hallandale...

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
DrugAugust 2, 2018· Pharmcore Inc.

Recalled Item: Ipamorelin 9 mg vial Lyophilized 1109 East Hallandale Beach Blvd. Recalled...

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
DrugAugust 2, 2018· Pharmcore Inc.

Recalled Item: Human Chorionic Gonadotropin 4000 IU Vial Lyophilized 1109 East Hallandale...

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
DrugAugust 2, 2018· Pharmcore Inc.

Recalled Item: Human Chorionic Gonadotropin 2500 IU Vial Lyophilized 1109 East Hallandale...

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
DrugAugust 2, 2018· Pharmcore Inc.

Recalled Item: Ipamorelin 3 mg Lyophilized 1 vial 1109 East Hallandale Beach Recalled by...

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
DrugAugust 2, 2018· Pharmcore Inc.

Recalled Item: Human Chorionic Gonadotropin 11000 IU Vial Lyophilized 1109 East Hallandale...

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
DrugAugust 2, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium tablets Recalled by Dr. Reddy's Laboratories, Inc. Due...

The Issue: Failed Impurities/Degradation Specifications - OOS was observed for ATV...

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

Class III — Low RiskOngoing
Refund
DrugAugust 1, 2018· American Health Packaging

Recalled Item: Doxycycline Hyclate Tablets Recalled by American Health Packaging Due to...

The Issue: Failed Dissolution Specifications: Out of specification result for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 1, 2018· Baxter Healthcare Corporation

Recalled Item: Levofloxacin Injection in 5% Dextrose Recalled by Baxter Healthcare...

The Issue: Superpotent Drug: High out of specification results for levofloxacin...

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

Class III — Low RiskOngoing
Refund
DrugAugust 1, 2018· Baxter Healthcare Corporation

Recalled Item: Levofloxacin Injection in 5% Dextrose Recalled by Baxter Healthcare...

The Issue: Superpotent Drug: High out of specification results for levofloxacin...

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

Class III — Low RiskOngoing
Refund
DrugAugust 1, 2018· Akorn, Inc.

Recalled Item: Lidocaine 2.5% and Prilocaine Cream Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurities/Degredation Specifications: Out of Specification results...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 1, 2018· Baxter Healthcare Corporation

Recalled Item: Levofloxacin Injection in 5% Dextrose Recalled by Baxter Healthcare...

The Issue: Superpotent Drug: High out of specification results for levofloxacin...

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

Class III — Low RiskOngoing
Refund
FoodAugust 1, 2018· Dole Fresh Vegetables Inc

Recalled Item: Dole Classic Coleslaw Recalled by Dole Fresh Vegetables Inc Due to Recall of...

The Issue: Recall of limited quantity of Classic Coleslaw due to potential for metal...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 1, 2018· COVIDIEN LLC

Recalled Item: Kerlix Bandage Roll Recalled by COVIDIEN LLC Due to Potential for product...

The Issue: Potential for product sterility breach due to a compromised or pinched seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2018· COVIDIEN LLC

Recalled Item: Kerlix Gauze Roll Recalled by COVIDIEN LLC Due to Potential for product...

The Issue: Potential for product sterility breach due to a compromised or pinched seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2018· COVIDIEN LLC

Recalled Item: Dermacea Gauze Fluff Roll Recalled by COVIDIEN LLC Due to Potential for...

The Issue: Potential for product sterility breach due to a compromised or pinched seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2018· EOS Imaging

Recalled Item: sterEOS workstation Recalled by EOS Imaging Due to 3D projections may be...

The Issue: 3D projections may be incorrect when the pair of images used is a secondary...

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

Class II — Potential Health HazardOngoing