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. 2,763 recalls have been distributed to New York in the last 12 months.
Showing 16621–16640 of 30,153 recalls
Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...
The Issue: The suction valve may not close properly which could cause continuous suction.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...
The Issue: The suction valve may not close properly which could cause continuous suction.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...
The Issue: The suction valve may not close properly which could cause continuous suction.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydroline Trumpet Valve with Pulse Wave Cassette Recalled by Cardinal Health...
The Issue: The suction valve may not close properly which could cause continuous suction.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRSASelect Recalled by Bio-Rad Laboratories, Inc Due to Abnormal coloration...
The Issue: Abnormal coloration of agar plates and the growth of non-characteristic MRSA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRSASelect II Recalled by Bio-Rad Laboratories, Inc Due to Abnormal...
The Issue: Abnormal coloration of agar plates and the growth of non-characteristic MRSA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCOS Modular Revision Hip System Recalled by Zimmer Biomet, Inc. Due to Two...
The Issue: Two lots of the Echo BI-Metric Hip Stem and ARCOS Modular Revision Hip Stem...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECHO Bi-Metric Hip System Recalled by Zimmer Biomet, Inc. Due to Two lots of...
The Issue: Two lots of the Echo BI-Metric Hip Stem and ARCOS Modular Revision Hip Stem...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dermatone AN Recalled by Zimmer Surgical Inc Due to Devices may have...
The Issue: Devices may have a loose control bar, which could compromise the ability to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare MRI Systems Recalled by GE Medical Systems, LLC Due to The...
The Issue: The latest on-site software version may not have been reinstalled at some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare MRI Systems Recalled by GE Medical Systems, LLC Due to The...
The Issue: The latest on-site software version may not have been reinstalled at some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare MRI Systems Recalled by GE Medical Systems, LLC Due to The...
The Issue: The latest on-site software version may not have been reinstalled at some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.