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. 2,869 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 6841–6860 of 29,947 recalls
Recalled Item: Samsung GM85 Digital X-ray Imaging System-A Digital Diagnostic Mobile X-ray...
The Issue: Issue related to the operation of the arm latch within the column that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REX (Recovery Exercise X-Trainer) Pressure Therapy System- USER Manual....
The Issue: Error in the Introduction section of the user manual that indicates the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EARLYVUE VS30 VITAL SIGNS MONITOR Software Version A.00.02 and A.00.01...
The Issue: EarlyVue VS30 Vital Signs Monitor and EarlyVue VS30 Vitals monitor Missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EarlyVue VS30 Vitals monitor with Software Versions A.00.02 and A.00.01...
The Issue: EarlyVue VS30 Vital Signs Monitor and EarlyVue VS30 Vitals monitor Missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System Recalled by Maquet...
The Issue: Some batches of product were not sterilized to their minimum sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VASOVIEW HEMOPRO Recalled by Maquet Cardiovascular, LLC Due to Some batches...
The Issue: Some batches of product were not sterilized to their minimum sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System Recalled by Maquet...
The Issue: Some batches of product were not sterilized to their minimum sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost N90 R.1.0 Recalled by Philips North America Due to Philips has...
The Issue: Philips has identified a compliance issue where ProxiDiagnost N90 R.1.0,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 R.1.0 Recalled by Philips North America Due to Philips has...
The Issue: Philips has identified a compliance issue where ProxiDiagnost N90 R.1.0,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 R1.1 Recalled by Philips North America Due to Philips has...
The Issue: Philips has identified a compliance issue where ProxiDiagnost N90 R.1.0,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SafeLight Fiber Optic Cable: Clear Recalled by Stryker Corporation Due to...
The Issue: Fiber optic cables assembled with not enough epoxy on the proximal end,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion CirClamp with 1.3cm Bell & Insert Reprocessed Recalled by MEDLINE...
The Issue: The CirClamp subassembly found in the kit was the incorrect size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NanoKnife 5-Probe Procedure Pack 15 cm - Activation. Indicated for Recalled...
The Issue: Not programmed in accordance with specification. The programming affects the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Pump Assembly Recalled by Coloplast Manufacturing US, LLC Due to A...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan NB Scrotal Zero Ang 18cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Touch NB Scrot Zero 18cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Touch Scro Zero Ang 22cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Touch Scro Zero Ang 20cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Step Bladeless Trocars Recalled by Covidien, LP Due to Medtronic was made...
The Issue: Medtronic was made aware of a supplier calibration issue during the contract...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan 0-Deg Scrotal 20 Cm Recalled by Coloplast Manufacturing US, LLC Due to XXX
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.