Product Recalls in Rhode Island
Product recalls affecting Rhode Island — including food, drugs, consumer products, medical devices, and vehicles distributed to Rhode Island. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,351 recalls have been distributed to Rhode Island in the last 12 months.
Showing 30541–30560 of 47,970 recalls
Recalled Item: 11cm 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: Rotating Adult Craniotome 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: Foot Control without Switches 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: Reciprocating MICRO SAW 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: Keyless Driver 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: 14cm 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: Electric Handpiece EM Hand Control Product Usage: Electric 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: 6.8cm Controlled Depth 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: SMALL 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: IMRI AIR CONTROL 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: 14cm QD Angle Attachment Product Usage: Product attachment 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: XMAX Motor 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: 12.6CM TAPERED ATTACHMENT 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: System Console 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: STANDARD CRANIOTOME 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: System Console 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: Rotating Large Craniotome 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: BLACKMAX-NEURO LOW PRESSURE 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: Bearing Sleeve 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: 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.