Stryker Sustainability Solutions recalls BARD Dynamic Tip Steerable
Incomplete seals on sterile product
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Showing 97–108 of 816 recalls
Incomplete seals on sterile product
Incomplete seals on sterile product
Incomplete seals on sterile product
Out-of-specification endotoxin result that did not meet the acceptance criteria.
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Potential for mislabeled syringe produced by the i.v.STATION device.
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles;…
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles;…
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles;…