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.
Showing 29021–29040 of 29,947 recalls
Recalled Item: Trabecular Metal Reverse Shoulder Liner 40mm Recalled by Zimmer, Inc. Due to...
The Issue: Lot specific Trabecular Metal (TM) Reverse Shoulder Liner Impactors are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shiley Reusable Cannula Low Pressure Cuffed Tracheostomy Tubes Recalled by...
The Issue: Covidien is recalling certain cuffed Shiley tracheostomy tubes due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00-4309-028-01 - Trabecular Metal Reverse Shoulder Liner 40mm 65¿ Neck...
The Issue: Lot specific Trabecular Metal (TM) Reverse Shoulder Liner Impactors are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00-4309-029-01 - Trabecular Metal Reverse Shoulder Liner 36 mm 65¿¿ Recalled...
The Issue: Lot specific Trabecular Metal (TM) Reverse Shoulder Liner Impactors are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo Imaging XS. Radiological image processing system. Recalled by Siemens...
The Issue: There is a potential malfunction when using syngo Imaging XS, version VA70A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00-4309-029-00- Trabecular Metal Reverse Shoulder Liner 36mm Recalled by...
The Issue: Lot specific Trabecular Metal (TM) Reverse Shoulder Liner Impactors are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RF Cannula Recalled by Stryker Instruments Div. of Stryker Corporation Due...
The Issue: Stryker has received 6 complaints that the 5mm needle was placed in 10 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista(R) Vancomycin Flex(R) Reagent Cartridge (VANC Recalled by...
The Issue: Siemens has received complaints of customers experiencing slopes >1.05 when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RF Cannula Recalled by Stryker Instruments Div. of Stryker Corporation Due...
The Issue: Stryker has received 6 complaints that the 5mm needle was placed in 10 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension(R) Reagent Management System (RMS) - Power Cord. The Siemens...
The Issue: Siemens Healthcare Diagnostics has confirmed that partial insertion of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur¿ Syphilis (SYPH) Assay Recalled by Siemens Healthcare...
The Issue: Syphilis Assay Interference with HBsAg Assay
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conformis iTotal CR-Cruciate Retaining Knee Replacement System Model...
The Issue: Addendum Labeling iTotal CR Surgical Technique with Detailed Instructions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DataCara GM is an information management system that provides data Recalled...
The Issue: Roche Molecular Systems, Inc. has become aware of a device-associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Special Orthopaedic Solution Peri-Acetabular Prosthesis V40 Femoral...
The Issue: Stryker has become aware that insufficient taper torsional strength may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The COBAS INTEGRA 400/400 plus system (software version 3.4) is Recalled by...
The Issue: Roche Molecular Systems, Inc. has become aware of a device-associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Data Station AMPLILINK software is an instrument user interface/ data...
The Issue: Roche Molecular Systems, Inc. has become aware of a device-associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DataInnovations (Instrument Manager) (version 8.04) interfaces middleware...
The Issue: Roche Molecular Systems, Inc. has become aware of a device-associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The COBAS 8000 data manager modular analyzer series (all versions) Recalled...
The Issue: Roche Molecular Systems, Inc. has become aware of a device-associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The MagNA Pure LC (version 3.0) is a sample preparation Recalled by Roche...
The Issue: Roche Molecular Systems, Inc. has become aware of a device-associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LightCycler 2.0 Instrument (software version 4.1) is a Rapid PCR Recalled by...
The Issue: Roche Molecular Systems, Inc. has become aware of a device-associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.