Product Recalls in Pennsylvania

Product recalls affecting Pennsylvania — including food, drugs, consumer products, medical devices, and vehicles distributed to Pennsylvania. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,722 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
2,722 in last 12 months

Showing 2014120160 of 29,947 recalls

Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: Large 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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: 8cm QD 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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: 13.5CM 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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: 26.65CM 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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: Autolube-III with 20ft hose 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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: eMax2 PLUS Product Usage: Electric 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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: IMRI CRANI-A 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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· Soft Computer Consultants, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: 5.0cm Heavy Duty Short Attachment Recalled by The Anspach Effort, Inc. Due...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· Soft Computer Consultants, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

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.

Class II — Potential Health HazardOngoing