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 2576125780 of 29,947 recalls

Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems TSH3 Ultra 2500 tests Catalog Number: 04862625...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems TSH3 Ultra Ready Pack Recalled by Siemens Healthcare...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems BRAHMS PCT 100 test Sold only OUS Recalled by Siemens...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Synthes, Inc.

Recalled Item: Synthes External Fixation Systems (Small Recalled by Synthes, Inc. Due to...

The Issue: Labeling changes have been made related to MR (Magnetic Resonance imaging)...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems TSH3 Ultra Recalled by Siemens Healthcare Diagnostics,...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems VitD 500 test Recalled by Siemens Healthcare...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems VitD Total 100 test Recalled by Siemens Healthcare...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2014· Cochlear Americas Inc.

Recalled Item: Cochlear Baha Soft tissue gauge 6mm. Reusable instrument used to Recalled by...

The Issue: Cochlear America is recalling Cochlear Baha Soft Tissue Gauge due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to When the E-NMT-01 module...

The Issue: When the E-NMT-01 module is used in conjunction with the ElectroSensor, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2014· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Fem-Flex II Arterial and femoral Cannulae with Duraflo...

The Issue: Potential for separation of dilator tips.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2014· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Fem-Flex II Arterial and femoral Cannulae Recalled by...

The Issue: Potential for separation of dilator tips.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: e.cam -emission computed tomography system Used to detect or image Recalled...

The Issue: There is a potential for patient finger injury on the e.cam systems.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2014· Philips Medical Systems, Inc.

Recalled Item: Intended for both adult and pediatric patients for taking diagnostic...

The Issue: In special cases, during the start-up of the current model of MobileDiagnost...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2014· Beckman Coulter, Inc.

Recalled Item: MicroScan Pos Combo Panel Type 33 (PC33): Catalog number B1017-211 Recalled...

The Issue: Siemens investigation confirmed that a portion one lot of panel Pos Combo 33...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2014· Small Bone Innovations, Inc.

Recalled Item: SBi RingFix Olive Wires Product Usage: These are temporary devices Recalled...

The Issue: Small Bone Innovations (SBI) is recalling non-sterile RingFIX Olive Wires...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2014· Abbott Laboratories, Inc

Recalled Item: Lipase Reagent Recalled by Abbott Laboratories, Inc Due to Package inserts...

The Issue: Package inserts have incorrect SmartWash parameters for Triglyceride.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2014· Laurimed LLC

Recalled Item: PolypVac 3.5mm Microdebrider Recalled by Laurimed LLC Due to The...

The Issue: The reciprocation mechanism in the PolypVac Microdebrider may turn off...

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

Class III — Low RiskOngoing
Medical DeviceApril 7, 2014· Western / Scott Fetzer Company

Recalled Item: Model RG3000 and RG4000 Series Valve Integrated Pressure Regulator (VIPR)...

The Issue: Separation events have occurred, including the VIPR separating from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2014· JAS Diagnostics Inc.

Recalled Item: Glucose Hexokinase Liquid Reagent For the in vitro quantitative...

The Issue: JAS Diagnostics, Inc. of Miami Lakes, FL is recalling their Glucose...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2014· Steris Corporation

Recalled Item: Vertical Spring Arm for Single or Dual Monitor Mount (Harmony Recalled by...

The Issue: Potential for the welded seam in affected monitor spring arms to crack...

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

Class II — Potential Health HazardOngoing