🏥 Medical Devices Class I - Dangerous
Limited access to flow settings as a result of the control knob having been rotated beyond its functional range
All Recalls
95,038 total recalls in our database
Argon Medical Devices AHD Luer Lock Cap, REF 501303, 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
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
The instrument holder may be sent on a trajectory that is not within the intended target. If it is not corrected, the associated device may be placed incorrectly.
🏥 Medical Devices Class I - Dangerous
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
🏥 Medical Devices Class I - Dangerous
A portion of the lot was incorrectly packaged with a 12.5cm catheter instead of a 15cm catheter.
Cardinal Health Brand 120mL/53mm sterile specimen container with orange cap, 75 pieces/pack, 4 packs/case Catalog number: CHB13904
Thermo Fisher Scientific (Monterrey)
🏥 Medical Devices Class I - Dangerous
Cardinal Health branded specimen containers, may potentially contain plastic shavings on threaded surfaces between the closure and vial
VITROS chemistry Products Cl- Slides, Catalog No. 6844471 (which supports Urine CL-). MicroSlides which contain reagents in a dry, multi-layered form.
Ortho-Clinical Diagnostics
🏥 Medical Devices Class I - Dangerous
Users may experience intermittent slide dispense issues with some cartridges due to the anti-backup platen failing to advance inside the cartridge.
🏥 Medical Devices Class I - Dangerous
Limited access to flow settings as a result of the control knob having been rotated beyond its functional range
Petfine Auto Injector, REF 3310VET
Owen Mumford USA
🏥 Medical Devices Class I - Dangerous
There is a possible assembly error on Autoject EI, lot number V14. This lot was packed into two products: AJ 1310, lot number V14 and AN 3310VET (branded as Petfine Auto Injector), batches V14.V976 & V14.W107
SPIFE Alkaline Hemoglobin Kit, Cat. No. 3415, for use in the separation and quantitation of hemoglobins by agarose electrophoresis using the SPIFE systems
Helena Laboratories
🏥 Medical Devices Class I - Dangerous
Lots of gel kits contained a newer revision of the Customer Procedures instructions than intended. The incorrect inserts refer to updated parameters associated with new electrodes -- which have not yet been made available to users.
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.
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
There is a potential security vulnerability related to the use of the remote controller accessories with the insulin pumps.
Hemo-Drop Blood Dispenser, Part Number BMP-HEMODROP, 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.
🏥 Medical Devices Class I - Dangerous
Limited access to flow settings as a result of the control knob having been rotated beyond its functional range
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).
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.