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. 2,679 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
2,679 in last 12 months

Showing 2914129160 of 29,947 recalls

Medical DeviceJune 26, 2012· Bridgepoint Medical

Recalled Item: BridgePoint Medical Recalled by Bridgepoint Medical Due to BridgePoint...

The Issue: BridgePoint Medical Inc. is voluntarily recalling Stingray Catheter, Model...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential issue due to an...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2012· Linvatec Corp. dba ConMed Linvatec

Recalled Item: NP211H***2009-02***CONMED LINVATEC 11311 CONCEPT BLVD LARGO Recalled by...

The Issue: Linvatec Corporation dba ConMed Linvatec in Largo, FL is recalling PressFT...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2012· Linvatec Corp. dba ConMed Linvatec

Recalled Item: "***PressFT***2.1 w/ Two #0 (3.5 metric)...

The Issue: Linvatec Corporation dba ConMed Linvatec in Largo, FL is recalling PressFT...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2012· Linvatec Corp. dba ConMed Linvatec

Recalled Item: "***PressFT***2.6 w/ Two #1 (4 metric)...

The Issue: Linvatec Corporation dba ConMed Linvatec in Largo, FL is recalling PressFT...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2012· Sunrise Medical (US) LLC

Recalled Item: Padded Swing Away Arm Rest with Receiver Recalled by Sunrise Medical (US)...

The Issue: Reports of injury when the Padded Swing Away Armrest is used for full body...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base 100/120V The Terumo Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received reports of various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base 220/240V. The Terumo Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received reports of various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base 100/120V The Terumo Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received reports of various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base 220/240V The Terumo Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received reports of various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Central Control Module for System 1: System 1 Base Recalled by Terumo...

The Issue: Terumo CVS has received reports of the Central Control Monitor (CCM) for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 Electronic O2 Blender/Analyzer. The...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) received two complaints related...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base Recalled by Terumo Cardiovascular Systems Corporation Due to...

The Issue: Terumo Advanced Perfusion System 1 battery charge is being depleted faster...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 System 1 Base Recalled by Terumo...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) received two complaints related...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base Recalled by Terumo Cardiovascular Systems Corporation Due to...

The Issue: Terumo Advanced Perfusion System 1 battery charge is being depleted faster...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base 220/240V The Terumo¿ Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) received eight complaints since...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base 100/120V The Terumo¿ Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) received eight complaints since...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Central Control Module for System 1: System 1 Base Recalled by Terumo...

The Issue: Terumo CVS has received reports of the Central Control Monitor (CCM) for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 System 1 Base Recalled by Terumo...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) received two complaints related...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base Recalled by Terumo Cardiovascular Systems Corporation Due to...

The Issue: Terumo¿ Advanced Perfusion System 1 has displayed a Red X error message on...

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

Class II — Potential Health HazardOngoing