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. 2,729 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,729 in last 12 months

Showing 74017420 of 53,528 recalls

Medical DeviceNovember 28, 2023· Medtronic Navigation, Inc.

Recalled Item: Medtronic Recalled by Medtronic Navigation, Inc. Due to Their is the...

The Issue: Their is the potential that the percutaneous pin may have a cross-pin that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2023· Medtronic Navigation, Inc.

Recalled Item: Medtronic Recalled by Medtronic Navigation, Inc. Due to Their is the...

The Issue: Their is the potential that the percutaneous pin may have a cross-pin that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2023· Natus Medical Incorporated

Recalled Item: EDS 3 CSF External Drainage System Recalled by Natus Medical Incorporated...

The Issue: Sterility assurance cannot be guaranteed for external drainage systems due...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2023· Natus Medical Incorporated

Recalled Item: External Drainage System Collection Bag Recalled by Natus Medical...

The Issue: Sterility assurance cannot be guaranteed for external drainage systems due...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2023· Mirion Technologies (Capintec), Inc.

Recalled Item: Captus 4000e Thyroid Uptake Systems- Intended to be used by Recalled by...

The Issue: Spring arm failure with Captus 4000e Thyroid Uptake Systems, can cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2023· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Immunodiagnostic Products Anti-HBs Quantitative Reagent Pack Recalled...

The Issue: Affected lots may experience increased calibration failures or an increase...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2023· Philips Respironics, Inc.

Recalled Item: Trilogy Evo and Trilogy Evo O2 Material Numbers BL2110X15B BR2110X18B...

The Issue: The following was missing from the Contraindications Statement: The AVAPS-AE...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2023· Acumed LLC

Recalled Item: RibLoc U Plus 90 Instrument PRIMARY GUIDE ASSY Recalled by Acumed LLC Due to...

The Issue: Due to potential breakage during use.

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

Class II — Potential Health HazardOngoing
FoodNovember 24, 2023· Houdini Inc.

Recalled Item: Acorn Raspberry Creme Filled Cookie found in gift basket: #197 Recalled by...

The Issue: Undeclared allergens; tree nuts

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 24, 2023· Houdini Inc.

Recalled Item: Acorn Raspberry Creme Filled Cookie found in gift basket: #359 Brownie...

The Issue: Undeclared allergens; tree nuts

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 24, 2023· Houdini Inc.

Recalled Item: Acorn Raspberry Creme Filled Cookie found in gift basket: #067 Believe...

The Issue: Undeclared allergens; tree nuts

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 24, 2023· Houdini Inc.

Recalled Item: Acorn Raspberry Creme Filled Cookie found in gift basket: #343 Brownie...

The Issue: Undeclared allergens; tree nuts

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 24, 2023· Houdini Inc.

Recalled Item: Acorn Raspberry Creme Filled Cookie found in gift basket: #342 Bakery...

The Issue: Undeclared allergens; tree nuts

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 24, 2023· Houdini Inc.

Recalled Item: Acorn Raspberry Creme Filled Cookie found in gift basket: #926 Recalled by...

The Issue: Undeclared allergens; tree nuts

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 24, 2023· Houdini Inc.

Recalled Item: Acorn Raspberry Creme Filled Cookie found in gift basket: #927 Recalled by...

The Issue: Undeclared allergens; tree nuts

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 24, 2023· Houdini Inc.

Recalled Item: Acorn Raspberry Creme Filled Cookie found in gift basket: #373 Cookie...

The Issue: Undeclared allergens; tree nuts

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 24, 2023· Houdini Inc.

Recalled Item: Acorn Raspberry Creme Filled Cookie found in gift basket: #925 Bakery...

The Issue: Undeclared allergens; tree nuts

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 23, 2023· FUJIFILM Healthcare Americas Corporation

Recalled Item: The device is a mobile x-ray system designed to work Recalled by FUJIFILM...

The Issue: When the key switch is turned on, the exposure conditions are set to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2023· ACTIM OY

Recalled Item: Actim PROM dipstik Recalled by ACTIM OY Due to Interference testing has...

The Issue: Interference testing has shown that the presence of personal lubricants in...

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

Class II — Potential Health HazardOngoing
DrugNovember 22, 2023· AnazaoHealth Corporation

Recalled Item: Thiamine HCl/Pyridoxine HCl 20 mg/mL /100mg/ml Injection Solution Recalled...

The Issue: Presence of Particulate Matter.

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

Class II — Potential Health HazardOngoing
Refund