🏥 Medical Devices Class I - Dangerous
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
All Recalls
95,038 total recalls in our database
🏥 Medical Devices Class I - Dangerous
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
Argon Medical Devices Septishield II, 80 cm, REF 497302, 25/box, Sterile, Rx. The firm name on the label is Argon Medical Devices, Inc., Athens, TX.
Argon Medical Devices
🏥 Medical Devices Class I - Dangerous
The seal formed on the edge of the pouch may be incomplete, which could result in a loss of sterility to the product.
🏥 Medical Devices Class I - Dangerous
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
🏥 Medical Devices Class I - Dangerous
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
🏥 Medical Devices Class I - Dangerous
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
CTSTM Essential 8 Medium
Life Technologies
🏥 Medical Devices Class I - Dangerous
Component was not tested by the supplier for adventitious agents
Manual Diff Dropper, Part Number CHB4001, used for preparing blood samples.
Biomedical Polymers
🏥 Medical Devices Class I - Dangerous
The metal cannula of the device either broke and the broken piece left in the blood specimen tube, or slid back into the plastic portion of the device instead of piercing the tube.
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
🏥 Medical Devices Class I - Dangerous
There is a potential security vulnerability related to the use of the remote controller accessories with the insulin pumps.
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
🏥 Medical Devices Class I - Dangerous
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
Forte Gamma Camera System is intended to produce images depicting the anatomical distribution of single-photon and positron-emitting radioisotopes within the body for interpretation by medical personnel.
Philips Medical Systems (Cleveland)
🏥 Medical Devices Class I - Dangerous
An issue with the Detector for the Forte Family of cameras may result in either detector 1 or detector 2 falling unimpeded vertically to the end stops of its travel limit.
🏥 Medical Devices Class I - Dangerous
This one pump shipped with incorrect pump programming, the initial production working version of the program. The pump would have immediately run at P9 for all selected P-levels, rather than a 10 second ramp up period. The pump may have migrated out of position and possibly caused injury. The positioning and suction alarms were also disabled.
Argon Medical Devices Plugs, Male/Female Luer Lock Plug, REF 041295000A, 50/box, Sterile, Rx. The firm name on the label is Argon Medical Devices, Inc., Athens, TX.
Argon Medical Devices
🏥 Medical Devices Class I - Dangerous
The seal formed on the edge of the pouch may be incomplete, which could result in a loss of sterility to the product.
🏥 Medical Devices Class I - Dangerous
BD has decided to initiate a voluntary recall due to a confirmed complaint trend for droplets of fluid separating from the sealed surface of the MaxZero connector, following disconnection.
Hitachi Scenaria Whole-body X-ray CT System
Hitachi Medical Systems America
🏥 Medical Devices Class I - Dangerous
There is a possibility that the cables to the controller unit may not be affixed properly, creating the potential for a cable to detach during scanning and eject from the system.
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
🏥 Medical Devices Class I - Dangerous
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).