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. 2,906 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 1441–1460 of 29,947 recalls
Recalled Item: Ingenia Ambition S Model Numbers (REF): (1) 781359 Recalled by Philips North...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 3.0T Recalled by Philips North America Due to The potential for...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Upgrade to MR 7700 Model Number (REF): 782130 Recalled by Philips North...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T CX Model Numbers (REF): (1) 781271 Recalled by Philips North...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition S Model Numbers (REF): (1) 781357 Recalled by Philips North...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva XR Recalled by Philips North America Due to The potential for...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to Ingenia Elition X Model Numbers (REF): (1) 782118 Recalled by...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura R8.2.x Systems. Software Verion: R8.2.x. 1. Allura Xper FD10...
The Issue: Potential for temporary loss of imaging (X-ray) functionality due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartSine SAM 350P Recalled by HeartSine Technologies Ltd Due to Due to a...
The Issue: Due to a component manufacturing issue, Automated External Defibrillator may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition X Model Numbers (REF): (1) 781356 Recalled by Philips North...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laser light show projectors manufactured by BLS Recalled by Beyond Laser...
The Issue: The remote interlock connector, which is required by 21 CFR 1040.10(f)(3),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laser light show projectors manufactured by BLS Recalled by Beyond Laser...
The Issue: The remote interlock connector, which is required by 21 CFR 1040.10(f)(3),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laser light show projectors manufactured by BLS Recalled by Beyond Laser...
The Issue: The remote interlock connector, which is required by 21 CFR 1040.10(f)(3),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sprinter Cart/Sprinter Cart XL Infusion Pole. Component used to hold...
The Issue: Device does not comply with the labeling requirements of international...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LYFO-DISK Recalled by Microbiologics Inc Due to KWIK-STIK : 0894P, 0894K and...
The Issue: KWIK-STIK : 0894P, 0894K and LYFO DISK" 0894L may result in failure to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Injection needle Recalled by Spiggle & Theis Mt Gmbh Due to Affected product...
The Issue: Affected product show elevated cytotoxicity values. Use of affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LYFO-DISK Recalled by Microbiologics Inc Due to KWIK-STIK : 0894P, 0894K and...
The Issue: KWIK-STIK : 0894P, 0894K and LYFO DISK" 0894L may result in failure to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPIDPoint 500 Systems Wash/Waste Cartridge (4 Pack). Material Number:...
The Issue: Siemens Healthcare Diagnostics is recalling the RAPIDPoint 500 Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breathing circuit set Recalled by Hamilton Medical AG Due to Ventilator...
The Issue: Ventilator coaxial breathing circuit may have a crack in blue tubing, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Base Recalled...
The Issue: Engaging titanium base was manufactured 180 degrees around the post from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.