Complete FDA and NHTSA recall records dated in 2025, organized for browsing by month, category and recalling company.
Select a month to review the recall records reported during that period.
Records are ordered by the best available source date.
Due to a potential open seal in the sterile barrier packaging.
The frequency inverter is not programmed by supplier according to specification which causes the circulation pump to start earlier than expected, resulting in additional wear and tear,…
In response to an increased number of reports of toxic anterior segment syndrome (TASS) in conjunction with implantation of enVista Aspire and enVista Envy IOLs, and certain enVista…
A software bug in Blueprint version 4.2.1 prevents users from accessing cases initiated in previous versions of the software.
Due to a potential open seal in the sterile barrier packaging .
The frequency inverter is not programmed by supplier according to specification which causes the circulation pump to start earlier than expected, resulting in additional wear and tear,…
Pumps may experience Wireless Connection Modules intermittent connection alarms, which will interrupt an active infusion. Interruption or delay of therapy can lead to serious patient injury…
Thrombectomy device specifies vessel range of 2.5-6 mm on the pouch, carton, and Instructions for Use rather than the correct vessel range of 3-6 mm, which could incrementally increase the…
There is a potential for thermal damage in CADD-Solis and CADD- Solis VIP infusion pumps.
Due to a potential open seal in the sterile barrier packaging .
There is a potential for thermal damage in CADD-Solis and CADD- Solis VIP infusion pumps.
Inadequate weld that can potentially cause the product to disassemble.
Due to a potential open seal in the sterile barrier packaging.
Affected pumps may trigger an erroneous (false) Upstream Occlusion Alarm under certain conditions, which will interrupt an active infusion. Interruption or delay of therapy can lead to…
Potential for exoskeleton to lose lateral balance and cause patient to fall.
Patient Monitor software update to address issues:1)May freeze at startup with MPM Application error and Attention Restart Required messages,2)Monitor may freeze and reboot at start of…
An issue was identified with the software when using the Echo Module of ISCV, the issue may result in missing or incomplete information in the report.
Affected pumps may trigger an erroneous (false) Upstream Occlusion Alarm under certain conditions, which will interrupt an active infusion. Interruption or delay of therapy can lead to…
Disconnection of the adapter from the endotracheal tube can potentially be difficult or not possible.
Ford Motor Company (Ford) is recalling certain 2022-2023 Bronco vehicles. The 360-degree view camera may not display a rearview image when the vehicle is placed in reverse.
Approximately 1mm to 8 mm sized pieces of foreign material (plastic) found in product.
Approximately 1mm to 8 mm sized pieces of foreign material (plastic) found in product.
Approximately 1mm to 8 mm sized pieces of foreign material (plastic) found in product.
Undeclared allergen ingredient (milk)
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.
