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. 1,184 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 2381–2400 of 29,947 recalls
Recalled Item: AlluraXper FD20 System Code: (1) 722006 (2) 722012 (3) 722028 Recalled by...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10C Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: Possibility of the patient falling from the table related to the mattress...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardio Vascular-Allura Centron Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...
The Issue: Possibility of the patient falling from the table related to the mattress...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Possibility of the patient falling from the table related to the mattress...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 5 M20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: Possibility of the patient falling from the table related to the mattress...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10/10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Possibility of the patient falling from the table related to the mattress...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 B20 System Code: (1) 722068 (2) 722226 (3) 722236 Recalled by...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 B12 System Code: (1) 722067 (2) 722225 (3) 722235 Recalled by...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 3 M12 System Code: (1) 722063 (2) 722221 Recalled by PHILIPS MEDICAL...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura CV20 System Code: 722031 Recalled by PHILIPS MEDICAL SYSTEMS...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: MediHoney¿ Gel Product Name: MediHoney¿ Wound & Burn Recalled by...
The Issue: Potential that the induction seal is not completely sealed to the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxC 500 AU Clinical Chemistry Analyzer Recalled by BECKMAN COULTER...
The Issue: Beckman Coulter has identified an issue which prevents the DxC 500 AU...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis: MedFlex Recalled by CareFusion 303, Inc. Due to Automated...
The Issue: Automated dispensing device labeling is being updated to strengthen labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: . Nobel Biocare N1 TiUltra TCC RP 4.0x9mm . Nobel Recalled by Nobel Biocare...
The Issue: Due to manufacturing issue (unintended by-product of the injection molding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Vascular Tack Endovascular System Recalled by Spectranetics...
The Issue: Use of Tack Endovascular system, designed to treat acute dissections of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CircuitGuard ThermoFlo Filter -Combined Heat and Moisture Exchanger Recalled...
The Issue: The machine side connector of the filter HME may be occluded by plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A820 myPTM Software Application associated with Medtronic SynchroMed Pump...
The Issue: Product complaints were received describing the A820 myPTM app taking longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CircuitGuard Bacterial/Viral Filter with Elbow (Model/Catalogue number:...
The Issue: The machine side connector of the filter HME may be occluded by plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Rapid fFN Specimen Collection Tube (PN: 71550-001) is a Recalled by...
The Issue: Three lots of Rapid fFN Specimen Collection kit (901164, 901165, and 904850)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) BD Pyxis MedStation ES Recalled by CareFusion 303, Inc. Due to Labeling...
The Issue: Labeling is insufficient regarding delays in access to medication. The firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.