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. 2,560 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,560 in last 12 months

Showing 2418124200 of 53,528 recalls

Medical DeviceFebruary 20, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS¿ 3600 Immunoassay System V3.3.2 & below Product Code: Recalled by...

The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS ECi Immunodiagnostic System Product Code: 6801059 For use Recalled by...

The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS¿ XT 7600 Integrated System-Software V3.4.1 & below Product Code:...

The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS¿ 3600 Immunoassay System-Software V3.3.2 & below Product Code:...

The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS¿ 5600 Integrated System -Software V3.3.2 & below Product Code:...

The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2019· Abbott Laboratories

Recalled Item: CELL-DYN Emerald analyzer Recalled by Abbott Laboratories Due to There is a...

The Issue: There is a potential for the device to generate Quality Control (QC) low or...

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

Class II — Potential Health HazardOngoing
FoodFebruary 20, 2019· Meijer

Recalled Item: Meijer Ultimate Chocolate Mint Chip Cookie Cookies in clear plastic Recalled...

The Issue: Undeclared soy

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 19, 2019· Beaver Visitec

Recalled Item: Micro Knife 5.0mm 30¿ Recalled by Beaver Visitec Due to The product contains...

The Issue: The product contains a misprinted expiration date on the peel pack. Both...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 19, 2019· Smith & Nephew, Inc.

Recalled Item: smith&nephew SMF(TM) STANDARD OFFSET STIKTITE(TM) COATED STEM 12/14 TAPER -1...

The Issue: Complaints were received indicating that the outer label incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2019· Smith & Nephew, Inc.

Recalled Item: smith&nephew SMF(TM) HIGH OFFSET STIKTITE(TM) COATED STEM 12/14 TAPER -1H...

The Issue: Complaints were received indicating that the outer label incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2019· Philips Medical Systems Nederlands

Recalled Item: Foot Switches used with Philips MultiDiagnost Eleva with Flat Detector...

The Issue: Additional units have been identified for previous recall Z-1280-2016 (RES...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2019· Philips Medical Systems Nederlands

Recalled Item: Foot Switches used with the following systems: 722001 Allura Xper Recalled...

The Issue: Additional units have been identified for previous recall Z-1280-2016 (RES...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2019· The Binding Site Group, Ltd.

Recalled Item: Optilite C-Reactive Protein Kit - Product Usage: The Optilite C-Reactive...

The Issue: Deterioration of C-reactive protein (CRP) reagent in Optilite C-Reactive...

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

Class II — Potential Health HazardOngoing
DrugFebruary 19, 2019· American Health Packaging

Recalled Item: Lovastatin Tablets USP Recalled by American Health Packaging Due to CGMP...

The Issue: CGMP Deviations: Finished product made with lovastatin drug substance that...

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 18, 2019· Avitus Orthopaedics, Inc.

Recalled Item: Avitus¿ Bone Harvester w/ Filter Insert - 5mm intended to Recalled by Avitus...

The Issue: Breach in the sterile barrier pouch may compromise sterility of the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2019· Avitus Orthopaedics, Inc.

Recalled Item: Avitus¿ Bone Harvester w/ Filter Insert - 8mm intended to Recalled by Avitus...

The Issue: Breach in the sterile barrier pouch may compromise sterility of the device.

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

Class II — Potential Health HazardOngoing
FoodFebruary 16, 2019· Concord Foods, LLC

Recalled Item: Concord Fresh Success Mild Salsa Seasoning Mix Recalled by Concord Foods,...

The Issue: Product contains undeclared allergen, milk.

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 15, 2019· Nature'S Path Foods Inc

Recalled Item: Nature's Path Organic Chocolate Choco Chimps Organic cereal. Net Wt....

The Issue: Gluten-free Cereals may contain undeclared gluten (wheat and barley).

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 15, 2019· Nature'S Path Foods Inc

Recalled Item: Nature's Path Organic Cinnamon Jungle Munch cereal. Net Wt. 10 oz (284 g)...

The Issue: Gluten-free Cereals may contain undeclared gluten (wheat and barley).

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 15, 2019· Nature'S Path Foods Inc

Recalled Item: Nature's Path Organic Gorilla Munch Corn Puffs cereal. Net Wt. 10 oz (284 g)...

The Issue: Gluten-free Cereals may contain undeclared gluten (wheat and barley).

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

Class II — Potential Health HazardOngoing
Refund