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. 2,691 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
2,691 in last 12 months

Showing 2404124060 of 29,947 recalls

Medical DeviceJanuary 15, 2015· Churchill Medical Systems, Inc.

Recalled Item: Bifurcated set with check vales and Bionectors Recalled by Churchill Medical...

The Issue: Potential for leaking caused by insufficient bond between needleless device...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2015· Churchill Medical Systems, Inc.

Recalled Item: 4" Microbore Double Lumen Set with Bionector Recalled by Churchill Medical...

The Issue: Potential for leaking caused by insufficient bond between needleless device...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2015· Abbott Laboratories, Inc

Recalled Item: ARCHITECT c4000 Cuvette Segment Recalled by Abbott Laboratories, Inc Due to...

The Issue: There is a potential to generate falsely-depressed patient results in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· INO Therapeutics (dba Ikaria)

Recalled Item: Ikaria Recalled by INO Therapeutics (dba Ikaria) Due to Potential delivery...

The Issue: Potential delivery failure alarm condition. INOmax DSIR with software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 101 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: ADAPTOR Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUA 540 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK SW/EAU STERILE Recalled by Teleflex Medical Due to Foreign Object...

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: Hudson RCI¿ Humidifier Adaptor Recalled by Teleflex Medical Due to Foreign...

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK SW/EAU STERILE Recalled by Teleflex Medical Due to Foreign Object...

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2015· GE Inspection Technologies, LP

Recalled Item: GE Inspection Technologies x|argos 160D system. Cabinet x-ray system....

The Issue: It was discovered that the upper left corner-shaped lead shield in the...

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

Class II — Potential Health HazardOngoing