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. 2,863 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
2,863 in last 12 months

Showing 79818000 of 29,947 recalls

Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner PC Hydrophilic Wire Guide PART NUMBER (RPN): RPC-35-180 Recalled...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWS-35-80...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWS-35-150...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWA-18-150...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner PC Hydrophilic Wire Guide PART NUMBER (RPN)RFPC-35-180 ORDER...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPW-35-150...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWA-35-150...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWA-18-80...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWAS-35-80...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWA-35-80...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS XT 7600 Integrated System with Version 3.7.2 and below Recalled by...

The Issue: Performing a system shutdown on VITROS XT 3400 and VITROS XT 7600 Systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS XT 3400 Chemistry System with Version 3.7.2 and below Recalled by...

The Issue: Performing a system shutdown on VITROS XT 3400 and VITROS XT 7600 Systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista LOCI CA 15-3 Flex reagent cartridge. In Vitro Recalled by...

The Issue: Negative bias with patient samples. The mean patient sample bias range from...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2022· Becton Dickinson & Company

Recalled Item: BD PhaSealTM Y-Site Connector (C80)- airtight and leak-proof Closed System...

The Issue: Incorrect expiration date listed on the product labels. The expiration date...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2022· DeRoyal Industries Inc

Recalled Item: DeRoyal limb holders: (1) DeRoyal Limb Holder Recalled by DeRoyal Industries...

The Issue: The webbing strap was laced improperly through the teeth of the buckle...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2022· GE Healthcare, LLC

Recalled Item: (1) GE Centricity Universal Viewer 6.0 Recalled by GE Healthcare, LLC Due to...

The Issue: Inaccurate Distance and Area measurements with use of Global Stack viewport.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2022· Philips Ultrasound, LLC

Recalled Item: Philips EPIQ Ultrasound Systems (various models) used in conjunction with...

The Issue: Retroactive: Ultrasound may experience an unexpected automatic reboot,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2022· Baxter Healthcare Corporation

Recalled Item: The Exacta-Mix 2400 compounding system Recalled by Baxter Healthcare...

The Issue: There is a potential for leaking valves on ports 1 to 4 in certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2022· Luminex Corporation

Recalled Item: ARIES SARS-CoV-2 Assay Recalled by Luminex Corporation Due to SARS-CoV-2...

The Issue: SARS-CoV-2 assay that detects SARS-CoV-2 ORF1ab and N genes may not detect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2022· Roche Diagnostics Operations, Inc.

Recalled Item: cobas e801 Immunoassay Analyzer Recalled by Roche Diagnostics Operations,...

The Issue: Software issue resulting in signals and sample test results of Pre-Wash...

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

Class II — Potential Health HazardOngoing