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. 929 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
929 in last 12 months

Showing 50781–50800 of 53,528 recalls

Medical DeviceDecember 20, 2012· Abbott Medical Optics Inc (AMO)

Recalled Item: AMO Sensar Intraocular Lenses (IOLs) Recalled by Abbott Medical Optics Inc...

The Issue: Two production orders of these IOLs that contain mislabeled IOLs.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Command Instrument Broach Handle. Used in Total Hip Arthroplasty. Catalog...

The Issue: Reports of handle fracture and subsequent disassociation of cam assembly...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2012· Healthtronics, Inc.

Recalled Item: HealthTronics Endocare 3.8mm RenalCryo Cryoprobe Recalled by Healthtronics,...

The Issue: The Endocare 3.8mm RenalCryo Cryoprobe is being recalled because the label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2012· Medisystems a NX Stage Company

Recalled Item: Medisystems 15 Gauge x 3/5 inch Buttonhole Needle Set Product Recalled by...

The Issue: A total of 5 (ea) single needle pouches are mislabeled as 15 Ga x1" instead...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: Philips MX 16-Slice CT Scanner System Recalled by Philips Medical Systems...

The Issue: The four screws that secure the patient table top to the carrier became...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2012· Elekta, Inc.

Recalled Item: Elekta Synergy XVI. Radiation Therapy Digital Imager. Product XVI R3.5.1...

The Issue: The DICOM tags do not contain sufficient information for XVI to identify the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2012· Hamilton Medical Inc

Recalled Item: HAMILTON-T1 Ventilator with software versions 1.1.2 or lower. The HAMILTON...

The Issue: Analysis of a customer complaint has shown that during ventilation of small...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista (R) Urinary/Cerebrospinal Fluid Protein (UCFP) Flex (R)...

The Issue: Siemens has confirmed an increase on absorbance errors when calibrating...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Leica Microsystems (Schweiz) Ag

Recalled Item: Surgical microscope The device is used to improve the visibility Recalled by...

The Issue: The brake in the Z axis and/or brakes in the AB and C axes failed during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Leica Microsystems (Schweiz) Ag

Recalled Item: Surgical microscope The device is used to improve the visibility Recalled by...

The Issue: The brake in the Z axis and/or brakes in the AB and C axes failed during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters Recalled by Cardinal Health Due to Small holes...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters Recalled by Cardinal Health Due to Small holes...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters Recalled by Cardinal Health Due to Small holes...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters Recalled by Cardinal Health Due to Small holes...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Abbott Laboratories, Inc

Recalled Item: ARCHITECT HBsAg Qualitative Assay Recalled by Abbott Laboratories, Inc Due...

The Issue: Abbott has identified that assay files for the ARCHITECT HBsAg Qualitative...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing