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 27181–27200 of 29,947 recalls
Recalled Item: LeGoo Internal Vessel Occluder .5mL Product Number: 10-0050 LeGoo is...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo¿ Endovascular Occlusion Gel-0.5 mL LeGoo with 3 Cannula Pouch Recalled...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo¿ Endovascular Occlusion Gel-2.5 mL LeGoo with 1 Cannula Pouch Recalled...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo Internal Vessel Occluder 1mL Product Number: 10-0100 LeGoo is Recalled...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TEG 5000 Thromboelastograph Coagulation Analyzer Product Usage: Multipurpose...
The Issue: Research Use Only (RUO) parameters were included in TEG 5000 User Manual.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beekley Spots Light Image O-Spots for Mammography Catalog Number: 252...
The Issue: Light Image O-Spots Dispenser mislabeled as Soft n' Stretchy Light Image S-Spots
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX Revolution Recalled by Carestream Health Inc. Due to Carestream Health...
The Issue: Carestream Health Inc. is conducting a recall for the Column end Cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Free Lock Femoral Hip Fixation System Compression Lag Screw . Recalled by...
The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSA-FX II FEMORAL FIXATION SYSTEM COMPRESSION TUBE/PLATE Recalled by...
The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Suction Wand Recalled by Edwards Lifesciences, LLC Due...
The Issue: Edwards is recalling certain lots of Rigid Suction Wands because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSA-FX II FEMORAL FIXATION SYSTEM COMPRESSION TUBE/PLATE Recalled by...
The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSA-FX FEMORAL FIXATION SYSTEM COMPRESSION LAG SCREW Recalled by Zimmer,...
The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 500 and Dimension Vista 1500 System Aliquot Well Recalled by...
The Issue: Siemens is conducting a field correction for Dimension Vista 500 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Free Lock Femoral Hip Fixation System Compression Tube/Plate Recalled by...
The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Recalled by Philips Healthcare...
The Issue: The MRx may deliver a non-synchronized cardioversion shock resulting in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Discovery IGS 730 Cardiovascular X-Ray Imaging System. The...
The Issue: GE Healthcare has recently become aware of a potential safety issue with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CHAMPION Medical Recliner Recalled by Invacare Corporation Due to There is a...
The Issue: There is a possibility of elevated temperatures in the seat pad. In...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeShield Recalled by Hospira Inc. Due to Hospira has received reports of...
The Issue: Hospira has received reports of customers experiencing air-in-line alarms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AlboGraft Knitted with Collagen Recalled by LeMaitre Vascular, Inc. Due to...
The Issue: Blood blushing/leaking from the surface of the graft after implantation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC unit Recalled by CareFusion 303, Inc. Due to CareFusion is...
The Issue: CareFusion is recalling the Alaris PC units model 8015 (PC unit), version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.