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. 2,547 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,547 in last 12 months

Showing 2818128200 of 53,528 recalls

Medical DeviceJanuary 31, 2018· Cook Inc.

Recalled Item: StoneBreaker C02 Cartridge Recalled by Cook Inc. Due to The interior of the...

The Issue: The interior of the product may not be sterilized to the appropriate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2018· Cook Inc.

Recalled Item: StoneBreaker Probe Cap Recalled by Cook Inc. Due to The interior of the...

The Issue: The interior of the product may not be sterilized to the appropriate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2018· Cook Inc.

Recalled Item: StoneBreaker Exhaust Line Recalled by Cook Inc. Due to The interior of the...

The Issue: The interior of the product may not be sterilized to the appropriate...

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

Class II — Potential Health HazardOngoing
DrugJanuary 30, 2018· Millennium Pharmaceuticals Inc.

Recalled Item: VELCADE (bortezomib) for injection Recalled by Millennium Pharmaceuticals...

The Issue: Defective Container: Confirmed reports of loose vial crimps.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 30, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ Calcium Flex¿ reagent cartridge Recalled by Siemens...

The Issue: May produce erroneously low results from specific well sets.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2018· Howmedica Osteonics Corp.

Recalled Item: Triathlon Revision Knee Catalog #5545-A-301 and Catalog #5546-A-601 The knee...

The Issue: Customers may receive the incorrect size implant from what is labeled on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2018· Encore Medical, Lp

Recalled Item: AltiVate Reverse INSTRUMENTATION Recalled by Encore Medical, Lp Due to...

The Issue: Broken or missing screws and retaining clips. This may be due to screw...

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

Class II — Potential Health HazardOngoing
DrugJanuary 29, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets 40 mg Recalled by Dr. Reddy's Laboratories,...

The Issue: Failed Impurities/Degradations Specifications; out-of-specification results...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2018· Teva Pharmaceuticals USA

Recalled Item: Fentanyl Transdermal System. 25 mcg/h Recalled by Teva Pharmaceuticals USA...

The Issue: Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO)...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2018· Teva Pharmaceuticals USA

Recalled Item: Fentanyl Transdermal System Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO)...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2018· Teva Pharmaceuticals USA

Recalled Item: Fentanyl Transdermal System Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO)...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2018· Mckesson Packaging Services

Recalled Item: Megestrol Acetate Oral Suspension Recalled by Mckesson Packaging Services...

The Issue: Subpotent Drug: Out of specification for assay (stability testing)

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

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2018· Teva Pharmaceuticals USA

Recalled Item: Fentanyl Transdermal System. 75 mcg/h Recalled by Teva Pharmaceuticals USA...

The Issue: Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO)...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets 10 mg Recalled by Dr. Reddy's Laboratories,...

The Issue: Failed Impurities/Degradations Specifications; out-of-specification results...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets 20 mg Recalled by Dr. Reddy's Laboratories,...

The Issue: Failed Impurities/Degradations Specifications; out-of-specification results...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 29, 2018· Beckman Coulter Inc.

Recalled Item: AQUIOS CL Flow Cytometer System Recalled by Beckman Coulter Inc. Due to The...

The Issue: The device may process the same sample with two different sample IDs and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Encore Medical, Lp

Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...

The Issue: It was discovered during a surgery that the design of the radius at the base...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Encore Medical, Lp

Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...

The Issue: It was discovered during a surgery that the design of the radius at the base...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Encore Medical, Lp

Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...

The Issue: It was discovered during a surgery that the design of the radius at the base...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Encore Medical, Lp

Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...

The Issue: It was discovered during a surgery that the design of the radius at the base...

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

Class II — Potential Health HazardOngoing