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. 2,741 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,741 in last 12 months

Showing 56215640 of 29,228 recalls

Medical DeviceSeptember 12, 2023· Beckman Coulter, Inc.

Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...

The Issue: The firm has investigated and confirmed that when DxI 9000 is connected to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2023· Olympus Corporation of the Americas

Recalled Item: THUNDERBEAT Recalled by Olympus Corporation of the Americas Due to...

The Issue: Thunderbeats blue seal button may remain in the engaged position after the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2023· Olympus Corporation of the Americas

Recalled Item: THUNDERBEAT Recalled by Olympus Corporation of the Americas Due to...

The Issue: Thunderbeats blue seal button may remain in the engaged position after the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2023· Ortho-Clinical Diagnostics, INc.

Recalled Item: VITROS Chemistry Products Lipase Slides Recalled by Ortho-Clinical...

The Issue: Products 1668409 and 8297749 may contain VITROS Lipase Slides with an...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2023· Siemens Medical Solutions USA, Inc

Recalled Item: ***Updated 12/4/23*** (1) Cios Flow (VA30) mobile fluoroscopic C-arm X-ray...

The Issue: Software issue for Cios Alpha, Cios Flow, and Cios Spin VA30 systems,...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2023· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Cios Alpha (VA30) mobile fluoroscopic C-arm X-ray System Recalled by...

The Issue: Software issue for Cios Alpha, Cios Flow, and Cios Spin VA30 systems,...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· EITAN MEDICAL LTD

Recalled Item: Sapphire Infusion Pumps Recalled by EITAN MEDICAL LTD Due to Infusion Pumps...

The Issue: Infusion Pumps with affected software revision may fail to detect air in...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing