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. 2,831 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
2,831 in last 12 months

Showing 1086110880 of 29,947 recalls

Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Tuohy-Borst Side-Arm Introducer (Shuttle Select) Recalled by Cook...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 23, 2020· Diasorin Inc.

Recalled Item: LIAISON 1-84 PTH Assay - Product Usage: is an in Recalled by Diasorin Inc....

The Issue: Potential for system to produce falsely elevated parathyroid hormone (PTH)...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: Naturalyte Liquid Acid concentrate bottles Recalled by Fresenius Medical...

The Issue: The deviation in conductivity for sodium level exceeds 0.6mS/cm from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: Naturalyte Liquid Acid concentrate bottles Recalled by Fresenius Medical...

The Issue: The deviation in conductivity for sodium level exceeds 0.6mS/cm from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· Baxter Healthcare Corporation

Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version...

The Issue: There is a potential software error during programming.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· B Braun Medical, Inc.

Recalled Item: APEX Compounding System Control Panel Module Recalled by B Braun Medical,...

The Issue: There is the potential for the compounding system to not immediately...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: Naturalyte Liquid Acid concentrate bottles Recalled by Fresenius Medical...

The Issue: The deviation in conductivity for sodium level exceeds 0.6mS/cm from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· Baxter Healthcare Corporation

Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version...

The Issue: There is a potential software error during programming.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· Baxter Healthcare Corporation

Recalled Item: Baxter Spectrum IQ Infusion System with Dose IQ Safety Software Recalled by...

The Issue: There is a potential software error during programming.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· Baxter Healthcare Corporation

Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version...

The Issue: There is a potential software error during programming.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: Citrasate Liquid Acid concentrate bottles Recalled by Fresenius Medical Care...

The Issue: The deviation in conductivity for sodium level exceeds 0.6mS/cm from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2020· B Braun Medical, Inc.

Recalled Item: APEX Compounding System Control Panel Module Recalled by B Braun Medical,...

The Issue: There is the potential for the compounding system to not immediately...

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

Class II — Potential Health HazardOngoing