Shire Human Genetic Therapies Natpara (parathyroid hormone) for Injection, 100 mcg, 2 pack recall — FDA D-0038-2020
Defective Delivery System: potential risk of rubber stopper particles clogging the needle and leading to underdosing
Browse the newest complete recall records currently stored from FDA enforcement reports and NHTSA vehicle campaigns. “Latest” refers to the newest source-dated record in this database, not the timestamp of our last API check.
The newest recall records with useful source details are listed here.
Defective Delivery System: potential risk of rubber stopper particles clogging the needle and leading to underdosing
Defective Delivery System: potential risk of rubber stopper particles clogging the needle and leading to underdosing
Ford Motor Company (Ford) is recalling certain 2020 Ford Explorer vehicles equipped with 2.3L or 3.3L engines. The wiring harness may not have been properly secured and may contact the air…
BMW of North America, LLC (BMW) is recalling certain 2018 540d, 2018-2020 530i, 530i xDrive, 540i, 540i xDrive, M550i xDrive, M5, 530e, 530e xDrive, X3 sDrive, X3 xDrive, X3 M40i, X3 M, and…
Honda (American Honda Motor Co.) is recalling certain 2019 CR-V vehicles. The owner's guide incorrectly describes when the "Passenger Airbag Off" indicator should illuminate. As such, these…
The sets are configured with quick connectors that have been assembled in reverse on the arterial and venous lines, resulting in blue (venous) to red (arterial) and red (arterial) to blue…
Remote Antenna Cable Used with Philips MX4O Monitors Does Not Have the Required Rating for Some Installations
Discrepancy between the correct expiration dates on the individual pouches inside the boxes and incorrect expiration dates on the outer boxes, where the month and day were reversed.
The inner diameter of the drill sleeve guide raw material was found to be under tolerance, potentially resulting in the drill bit seizing in the guide during surgery.
Potential need for device replacement - Elective Replacement Indicator (ERI) or End of Life (EOL) - earlier than expected due to compromised performance of an electrical component causing…
Potential for Hemospray device to be unable to spray powder due to misassembly of devices.
Potential need for device replacement - Elective Replacement Indicator (ERI) or End of Life (EOL) - earlier than expected due to compromised performance of an electrical component causing…
Product has potential to be contaminated with Listeria monocytogenes
Product has potential to be contaminated with Listeria monocytogenes
Product has potential to be contaminated with Listeria monocytogenes
Product has potential to be contaminated with Listeria monocytogenes
Product has potential to be contaminated with Listeria monocytogenes
Product has potential to be contaminated with Listeria monocytogenes
Product has potential to be contaminated with Listeria monocytogenes
Product has potential to be contaminated with Listeria monocytogenes
Product has potential to be contaminated with Listeria monocytogenes
Product has potential to be contaminated with Listeria monocytogenes
Product has potential to be contaminated with Listeria monocytogenes
Product has potential to be contaminated with Listeria monocytogenes
Browse recent months with enough recall history for useful comparison.