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 25621–25640 of 29,947 recalls
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeVilbiss Model DV5x Series CPAP units. For use in treating Recalled by...
The Issue: A limited number of DV5x Series CPAP units were manufactured and shipped...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical TAMPA CATHETER 5 French 33 cm. Intended for Recalled by...
The Issue: Sterility of the device may be compromised due to unsealed pouch
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microline Surgical ReNew Laproscopic Fenestrated Grasper Forceps Tips...
The Issue: Potential for the Fenestrated Grasper Tip jaw to break when force is applied...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS (R) Chemistry Products Calibrator Kit 17 Recalled by Ortho-Clinical...
The Issue: Calibrator values assigned for the calibrator kit lots were released using a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS (R) Chemistry Products FS Calibrator 1 Recalled by Ortho-Clinical...
The Issue: Calibrator values assigned for the calibrator kit lots were released using a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microline Surgical ReNew Laproscopic Fenestrated Grasper Forceps Tips...
The Issue: Potential for the Fenestrated Grasper Tip jaw to break when force is applied...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba Infinix X-Ray Interventional System INFX-8000V/UU. An X-Ray system...
The Issue: Although the Flat Panel Detector (FPD) touch sensor is activated during use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Mobilett XP Digital Mobile X-ray System Product Usage: The Recalled...
The Issue: There is a potential fire hazard of certain Lithium-Ion batteries in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Ysio Systems Product Usage: The Ysio (New RAD-FAMILY) systems...
The Issue: Excessive usage of cleaning liquid on Siemens Ysio Systems may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 1000 defibrillator. Affected Part Numbers: 320371500XXX The LP1000...
The Issue: Physio-Control has become aware of incidents where customers have attempted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs Healthcare Ventilator Flexport Interface Recalled by Spacelabs...
The Issue: Spacelabs Healthcare is voluntarily recalling the Hamilton Galileo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.