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. 1,184 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 2301–2320 of 29,947 recalls
Recalled Item: ET Rigid Abutment (Mini) SIze: 4.5D 3.0G/H 7.0H - Intended Recalled by...
The Issue: Patient chart stickers provided inside the packaging may incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Osstem Implant System - Abutment: ET Multi AbutmentSize: 4.8D 5.0GH Recalled...
The Issue: Patient chart stickers provided inside the packaging may incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ET Rigid Abutment (Mini) Size: 4.5D 2.0G/H 4.0H- Intended for Recalled by...
The Issue: Patient chart stickers provided inside the packaging may incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: MiniDock Product Name: Integrated Nucleic Acid Testing Device...
The Issue: Devices were distributed in the U.S. market without obtaining the required...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Pluslife SARS-CoV-2 Card Product Name: SARS-CoV-2 Nucleic Acid...
The Issue: Devices were distributed in the U.S. market without obtaining the required...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Lumenis Pulse 120H 30 amp Recalled by LUMENIS, LTD. Due to The initial...
The Issue: The initial current in certain chargers may lead to overheating and damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris Pump Module The BD Alaris System Recalled by CareFusion 303, Inc....
The Issue: Due to User Manual/Direction for Use incorrectly instructing user to leave...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedFlex 2.0 Bio-ID Spare Parts by CareFusion 303, Inc. Due to Due...
The Issue: Due to fingerprint scanner failing resulting in the scanner heating up.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX -ANATOMIC LAT FIB PLATE 6H LT- Anatomic Lateral Fibula Plate...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX-P: ANATOMIC LAT FIB PLATE 12H LT- Anatomic Lateral Fibula Plate...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX-MEDIAL TIBIA PLATE 6H LT-Medial Tibia Plate Recalled by Tyber...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX--MEDIAL TIBIA PLATE 12H RT-Medial Tibia Plate Recalled by Tyber...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX-MEDIAL TIBIA PLATE 12H LT-Medial Tibia Plate Recalled by Tyber...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 35 ECG cable Recalled by Physio-Control, Inc. Due to Product shipped...
The Issue: Product shipped with incorrect IFU. IFU does not include proper...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX-MEDIAL TIBIA PLATE 10H RT-Medial Tibia Plate Recalled by Tyber...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX- Product Name: ANATOMIC LAT FIB PLATE 10H LT Recalled by Tyber...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX- MEDIAL TIBIA PLATE 10H LT- Medial Tibia Plate Recalled by...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 V4/Masimo Rainbow Sensors: Masimo¿ RD rainbow Adt 8¿ SpCO...
The Issue: Due to an error message that prevents users from utilizing carboxyhemoglobin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 6H RT: Anatomic Lateral Fibula Plate...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 8H LT: Anatomic Lateral Fibula Plate...
The Issue: Complaints of the locking screw passing through the locking hole...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.