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 85018520 of 53,528 recalls

Medical DeviceJuly 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton C1/T1/MR1 Recalled by Hamilton Medical, Inc. Due to Degrading...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton-T1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton-T1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton-T1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 26, 2023· Zimmer, Inc.

Recalled Item: M/L Taper Hip Prosthesis Extended Offset Recalled by Zimmer, Inc. Due to The...

The Issue: The outer package labeling and product etch are for a Size 6, however, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Link OptiStem Rasp Handle-Used with the OptiStem Rasp to prepare Recalled by...

The Issue: A crack in the weld of the rasp handle may lead to a fracture of the frontal...

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

Class II — Potential Health HazardOngoing
FoodJuly 25, 2023· The Sausage Maker, Inc.

Recalled Item: The Sausage Maker Instacure #1 Recalled by The Sausage Maker, Inc. Due to...

The Issue: Contains Sodium Nitrite recalled for potential metal contamination

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 25, 2023· SenTec AG

Recalled Item: Membrane Changer Single-Use Recalled by SenTec AG Due to During rework of...

The Issue: During rework of components during the manufacturing process, an additional...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2023· Diversatek Healthcare

Recalled Item: ZVU Functional GI Software Recalled by Diversatek Healthcare Due to GI...

The Issue: GI Software labelled as revision 3.3.0 is incorrectly labeled and is in fact...

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

Class III — Low RiskOngoing
Medical DeviceJuly 25, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by...

The Issue: There is a potential for ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2023· Medtronic Navigation, Inc.-Littleton

Recalled Item: The O-arm O2 Imaging System is a mobile x-ray system Recalled by Medtronic...

The Issue: Ground cable installed incorrectly.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2023· Cook Vandergrift, Inc.

Recalled Item: Cook Lead Clipper- An auxiliary tool indicated for use in Recalled by Cook...

The Issue: Sterility of device may be compromised due to breach of the chevron seal of...

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

Class II — Potential Health HazardOngoing
FoodJuly 22, 2023· Newly Weds Foods, Inc.

Recalled Item: Newly Weds Foods G25928 CURE 6.25% W/SALT W/O ADDITIVES X1 50lbs Recalled by...

The Issue: may contain small pieces of metal, approximately 1mm in size or less

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

Class III — Low RiskOngoing
Refund
FoodJuly 22, 2023· Newly Weds Foods, Inc.

Recalled Item: Newly Weds Foods R03810 LOEFFLER COMP PORK ROLL CURE X1 54lbs Recalled by...

The Issue: May contain small pieces of metal, approximately 1mm or less in size

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

Class III — Low RiskOngoing
Refund
FoodJuly 22, 2023· Newly Weds Foods, Inc.

Recalled Item: Newly Weds Foods R03361 HAHN'S SPECIAL BACON CURE HS X1 40lbs Recalled by...

The Issue: may contain small pieces of metal, approximately 1mm in size or less

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

Class III — Low RiskOngoing
Refund
FoodJuly 22, 2023· Newly Weds Foods, Inc.

Recalled Item: Newly Weds Foods R01395 HELLER'S MODERN CURE 50lbs Recalled by Newly Weds...

The Issue: may contain small pieces of metal, approximately 1mm in size or less

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

Class III — Low RiskOngoing
Refund
DrugJuly 21, 2023· The Ritedose Corporation

Recalled Item: Cromolyn Sodium Oral Solution (Concentrate) 100 mg/5 mL 96 Plastic Recalled...

The Issue: CGMP deviation: product released prior to supplier approval.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 21, 2023· Aurobindo Pharma USA Inc.

Recalled Item: Rufinamide Tablets Recalled by Aurobindo Pharma USA Inc. Due to cGMP...

The Issue: cGMP deviations: Batch was released prior to approval.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 21, 2023· Aurobindo Pharma USA Inc.

Recalled Item: Rufinamide Tablets Recalled by Aurobindo Pharma USA Inc. Due to cGMP...

The Issue: cGMP deviations: Batch was released prior to approval.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 21, 2023· Ambu Inc.

Recalled Item: Ambu aView 2 A Monitor-The Ambu aView 2 Advance is Recalled by Ambu Inc. Due...

The Issue: Multiple impacts, for example from being dropped, can cause to the Ambu...

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

Class II — Potential Health HazardOngoing