Product Recalls in New York

Product recalls affecting New York — including food, drugs, consumer products, medical devices, and vehicles distributed to New York. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,840 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,840 in last 12 months

Showing 89819000 of 55,896 recalls

Medical DeviceJuly 31, 2023· Datascope Corp.

Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...

The Issue: Users were experiencing a failure in the IAB Fiber Optic Sensor input on the...

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

Class II — Potential Health HazardOngoing
DrugJuly 27, 2023· ALEMBIC PHARMACEUTICALS, INC.

Recalled Item: Tobramycin Opthalmic Solution USP Recalled by ALEMBIC PHARMACEUTICALS, INC....

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 5F 100CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 8F 90CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 5F PRE-SHAPED 40 90CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 6F 90CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 6F PRE-SHAPED 40 90CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 5F 90CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 7F 100CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 8F PRE-SHAPED 40 90CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 8F 100CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 8F PRE-SHAPED 40 100CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 5F PRE-SHAPED 40 100CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 7F 90CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 6F 100CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 7F PRE-SHAPED 40 100CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 6F PRE-SHAPED 40 100CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 7F PRE-SHAPED 40 90CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Wolf, Henke Sass, Gmbh

Recalled Item: Henke-Ject-2 part luer sterile single use syringes - used for intravenous...

The Issue: Sterile barrier might be damaged compromising the sterility of the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Aomori Olympus Co., Ltd.

Recalled Item: Olympus Distal Attachment (in Olympus Disposable EMR Kit)- Designed to...

The Issue: The Distal Attachment contain di-2-ethylhexyl phthalate (DEHP), which...

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

Class II — Potential Health HazardOngoing