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.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
The hip cup liner that was packaged with the incorrect labeling. HDL-060-C22S-000101 from Lot 1788258 contained a hooded liner, but it was labeled to have a standard liner.
the impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
If "Clear All" selected medications is selected on patient profile, the automated dispensing cabinet may allow dispensing of medication without first requiring the RxVerify Validation Code…
The impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use.
Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
The battery for certain ultrasound systems can potentially develop an internal failure which could result in smoke or fire.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Lack of sterility assurance for closed suction catheter systems
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
the impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use.
Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
Lack of sterility assurance for closed suction catheter systems
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
A software defect in Version 7.9 of the pump software for Tandem t:slim X2 and Tandem Mobi pumps, when used with Control IQ+ technology, will cause the pump to incorrectly interpolate…
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.
