🏥 Medical Devices Class I - Dangerous
Due to internal venturi component getting transiently stuck in the forward position within the breathing circuit and may cause a reduction of amplitude and volume of ventilation.
All Recalls
92,900 total recalls in our database
🏥 Medical Devices Class I - Dangerous
The probe tips of the hand instruments are being damaged or breaking including pad damage and detachment.
BD Pyxis Med ES Auxiliary (AUX), REF 343
CareFusion 303
🏥 Medical Devices Class I - Dangerous
Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Situation 2: Cable Ribbon Damage, Situation 3: Magnet Falling Out,
🏥 Medical Devices Class I - Dangerous
Lack of 510(k) clearance.
🏥 Medical Devices Class I - Dangerous
There is potential the device inside the package may not match the product information on the outer label (e.g., label states 5820-107-430 but package contains a 5820-107-530 device or vice versa).
🏥 Medical Devices Class I - Dangerous
Potential for hole in package compromising sterility of the medical kit.
🏥 Medical Devices Class I - Dangerous
The probe tips of the hand instruments are being damaged or breaking including pad damage and detachment.
🏥 Medical Devices Class I - Dangerous
There is potential the device inside the package may not match the product information on the outer label (e.g., label states 5820-107-430 but package contains a 5820-107-530 device or vice versa).
🏥 Medical Devices Class I - Dangerous
The probe tips of the hand instruments are being damaged or breaking including pad damage and detachment.
🏥 Medical Devices Class I - Dangerous
Lack of 510(k) clearance.
Baxter Continu-Flo Solution Set with Duo-Vent Spike, REF UC8519
Baxter Healthcare
🏥 Medical Devices Class I - Dangerous
Specific lots of Solution Sets with Duo-Vent Spike have the potential for inverted side clamps causing the tubing to be unusable.
🏥 Medical Devices Class I - Dangerous
The probe tips of the hand instruments are being damaged or breaking including pad damage and detachment.
There is potential the device inside the package may not match the product information on the outer label (e.g., label states 5820-107-030 but package contains a 5820-107-530 device).
🏥 Medical Devices Class I - Dangerous
Sterility assurance; microcatheter inner packaging may contain incomplete seal.
BD PCR Cartridges used with MAX System. Model Number: 437519
Becton Dickinson &
🏥 Medical Devices Class I - Dangerous
Potential for signal drift in specific lots of BD PCR Cartridges.
DLP Pediatric One-Piece Arterial Cannulae, Model Numbers 77008 (8 Fr) and 77014 (14 Fr)
Medtronic Perfusion Systems
🏥 Medical Devices Class I - Dangerous
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
🏥 Medical Devices Class I - Dangerous
Elevated residues of anti-block/slip additive used in manufacturing found within sterile packaging.
🏥 Medical Devices Class I - Dangerous
Potential for hole in package compromising sterility of the medical kit.
🏥 Medical Devices Class I - Dangerous
Potential for hole in package compromising sterility of the medical kit.
🏥 Medical Devices Class I - Dangerous
Potential for hole in package compromising sterility of the medical kit.