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. 2,507 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,507 in last 12 months

Showing 3880138820 of 53,528 recalls

DrugAugust 17, 2015· Bausch & Lomb, Inc.

Recalled Item: Bromfenac Ophthalmic Solution Recalled by Bausch & Lomb, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Failed preservative effectiveness testing.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 14, 2015· Toshiba American Medical Systems Inc

Recalled Item: INFX-8000V Bi-Plane X-Ray Interventional System X-ray systems Recalled by...

The Issue: When a fontal DA (Digital Angiography) acquisition was done, scattered x-ray...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Edge Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...

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

Class II — Potential Health HazardOngoing
FoodAugust 14, 2015· Anhing Corporation

Recalled Item: Caravelle ABC Cookies Banh Chu NET WT: 7oz (200gr) Product of Vietnam...

The Issue: Anhing Corporation is recalling Caravelle ABC Cookies because recent...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2015· GlaxoSmithKline, LLC.

Recalled Item: Bactroban Ointment (mupirocin calcium) Recalled by GlaxoSmithKline, LLC. Due...

The Issue: Penicillin Cross Contamination and Presence of Foreign Substance. Product...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2015· GlaxoSmithKline, LLC.

Recalled Item: Mupirocin Calcium Cream Recalled by GlaxoSmithKline, LLC. Due to Penicillin...

The Issue: Penicillin Cross Contamination and Presence of Foreign Substance. Product...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· GlaxoSmithKline, LLC.

Recalled Item: Bactroban (mupirocin calcium) Nasal Ointment Recalled by GlaxoSmithKline,...

The Issue: Penicillin Cross Contamination and Presence of Foreign Substance. Product...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2015· GlaxoSmithKline, LLC.

Recalled Item: Bactroban Cream (mupirocin calcium) Recalled by GlaxoSmithKline, LLC. Due to...

The Issue: Penicillin Cross Contamination and Presence of Foreign Substance. Product...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 12, 2015· Abbott Electrophysiology

Recalled Item: FIRMap 60mm Catheter Recalled by Abbott Electrophysiology Due to The...

The Issue: The expiration date was incorrectly printed on the pouch/box labels of 19...

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

Class III — Low RiskOngoing
Medical DeviceAugust 11, 2015· Synthes (USA) Products LLC

Recalled Item: Dynamic Locking Screw System (DLS) 3.7mm & Dynamic Locking Screw (DLS) 5.0mm...

The Issue: DLS pin breakage during planned implant removal, after uneventful and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2015· Alcon Research, Ltd.

Recalled Item: LX3 Floor Stand for Endure Luxite Envision Optical System Recalled by Alcon...

The Issue: Alcon is initiating a voluntary recall of all LX3 Microscope Floor Stands...

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

Class II — Potential Health HazardOngoing