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. 2,619 recalls have been distributed to New York in the last 12 months.
Showing 35741–35760 of 55,896 recalls
Recalled Item: 20.2cm Heavy Duty Long Heavy Short Attachment Recalled by The Anspach...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Craniotome Product Usage: Pneumatic system Recalled by The Anspach...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRI SHORT ATTACHMENT Product Usage: Pneumatic system Recalled by The...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCC Soft Computer Softbank II software Product Usage: Supports single...
The Issue: Software error. Potential for incorrect results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AL-III W/ male disconnect and 30ft hose Product Usage: Pneumatic system...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electronic Foot Control with Direction or Irrigation Switches Product Usage:...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Softbank software Product Usage: Decision support software for transfusion...
The Issue: Software error. Potential for incorrect results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Autolube-III with NK Product Usage: Pneumatic system Recalled by The Anspach...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 90 degree Contra Angle Attachment Product Usage: Pneumatic system Recalled...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foot control irrigation system Product Usage: Pneumatic system Recalled by...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 22CM MICRO REVISION ATTACH Recalled by The Anspach Effort, Inc. Due to...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foot Control Recalled by The Anspach Effort, Inc. Due to Supplied Directions...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRI MOTOR Product Usage: Pneumatic system Recalled by The Anspach Effort,...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10.5cm QD Angle Attachment Product Usage: Pneumatic system Recalled by The...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 19cm Attachment Recalled by The Anspach Effort, Inc. Due to Supplied...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electronic Foot Control with Direction Switch Product Usage: Electric system...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compact Speed Reducer Recalled by The Anspach Effort, Inc. Due to Supplied...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eMax2 Hybrid Hand Control Product Usage: Electric system Recalled by The...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11CM ANGLE ATTACHMENT Recalled by The Anspach Effort, Inc. Due to Supplied...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AL-III-DISS Adapter Product Usage: Pneumatic system Recalled by The Anspach...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.