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 26161–26180 of 29,947 recalls
Recalled Item: GE Healthcare CARESCAPE Monitor B650 and CARESCAPE Monitor B850. The...
The Issue: GE Healthcare has recently become aware of potential safety issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vital Signs Anesthesia Circuits The Ventilator Circuit is intended for...
The Issue: A circuit in use was occluded by a blue port cap that was inadvertently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KODAK DirectView DR 7500 Dual Detector System Recalled by Carestream Health,...
The Issue: Carestream Health, Inc. has recalled DR 7500 Dual Detector System utilizing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Horizon Medical Imaging Recalled by Mckesson Information Solutions LLC Due...
The Issue: Images may be archived to an incorrect or invalid archive location resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON SC2000 Power Input: 100-240VAC Recalled by Siemens Medical Solutions...
The Issue: The locking mechanism that is intended to hold the control panel in a fixed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON SC2000 Ultrasound System Recalled by Siemens Medical Solutions USA,...
The Issue: The user interface assembly on the ACUSON SC2000 may become loose with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000/2000 XPi Systems Androstenedione (Test Code AND) Recalled by...
The Issue: Siemens Healthcare Diagnostics confirmed over-recovery of samples with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESCAPE Monitor B850 Recalled by GE Healthcare, LLC Due to There is a...
The Issue: There is a potential for communication loss associated with the F5-01 Frame...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalys Precision Laser System (United States) - Catalys-U: Catalys...
The Issue: Potential for unexpected heating of the transformer mounting bolt located...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orbit soft Infusion sets Recalled by Perrigo Diabetes Care Due to Perrigo...
The Issue: Perrigo was notified by our supplier, Ypsomed AG, that they are recalling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compensator Slider Lambda 6x20 component (part number 473704-0000-000)...
The Issue: Carl Zeiss Microscopy, LLC has recalled the Compensator Slider Lamda 6x20...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE/IMMULITE 1000 Systems Androstenedione (Test Code AND) Recalled by...
The Issue: Siemens Healthcare Diagnostics confirmed over-recovery of samples with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIFY¿ SixCess 270FP Challenge Pack Recalled by Steris Corporation Due to...
The Issue: STERIS has identified that the outer shipping package for one lot (Lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIATELE TELEMETRY TRANSMITTER Recalled by Spacelabs Healthcare, Llc Due to...
The Issue: The AriaTele Model 96281 with SpO2 monitoring Option C is recalled because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemochron Jr. Citrate APTT Cuvette 510(k) K014008 A unitized...
The Issue: ITC has determined that some Citrate APTT cuvettes may recover higher than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Segmental Systems Recalled by Zimmer, Inc. Due to After evaluation of...
The Issue: After evaluation of 13 complaints(0.4% rate) for hyper-extension of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Segmental Systems Recalled by Zimmer, Inc. Due to After evaluation of...
The Issue: After evaluation of 13 complaints(0.4% rate) for hyper-extension of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: On Site Gas Systems POGS 33C Portable Oxygen Generation System Recalled by...
The Issue: Heat exchanger hose becomes weak and may fail.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Weck Recalled by Teleflex Medical Due to Sterility cannot be guaranteed.
The Issue: Sterility cannot be guaranteed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Weck Recalled by Teleflex Medical Due to Sterility cannot be guaranteed.
The Issue: Sterility cannot be guaranteed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.