🏥 Medical Devices Class I - Dangerous
Complaints received of the front joint of the spring arm AC 2000 could break at the interface to the monitor.
All Recalls
95,114 total recalls in our database
🏥 Medical Devices Class I - Dangerous
The recalling firm has received reports of a malfunction of the Relax wall mounted shower seat where the wall bracket has cracked or broken.
🏥 Medical Devices Class I - Dangerous
AngioJet products were distributed with an incorrect use-by (expiry) date. The correct date is Nov-2015, but the units are labeled with a use-by date of Dec-2015.
Naturalyte Liquid Bicarbonate Concentrate 6.4 liter bottle A Dialysate Concentrate for Hemodialysis (liquid) Product Code: 08-4000-LB
Fresenius Medical Care Holdings
🏥 Medical Devices Class I - Dangerous
Expansion of recall to lots manufactured in 2015 due to the potential for bacterial contamination.
The firm received a complaint stating the Coil Extension Cable accessory would overheat and be a burn hazard if touched.
🏥 Medical Devices Class I - Dangerous
AngioJet products were distributed with an incorrect use-by (expiry) date. The correct date is Nov-2015, but the units are labeled with a use-by date of Dec-2015.
🏥 Medical Devices Class I - Dangerous
Complaints received of the front joint of the spring arm AC 2000 could break at the interface to the monitor.
🏥 Medical Devices Class I - Dangerous
Ventricular packing: LV software programming versions for BIOTRONIK CRT-P and CRT-D devices are recalled because they are not approved for use in the US.
🏥 Medical Devices Class I - Dangerous
A reagent present may produce weak or slow reactions; continued use may result in a failure to identify target species.
🏥 Medical Devices Class I - Dangerous
The batteries used in the Invacare¿ Pronto¿ Air Personal Transporter models power wheelchairs have the possibility to overheat during charging which could potentially result in leaking battery acid and/or swelling battery, loss of use, chemical burns and/or property damage.
ReSolve Locking Drainage Catheters The ReSolve Locking Catheters are intended for percutaneous drainage of fluids from body cavities.
Merit Medical Systems
🏥 Medical Devices Class I - Dangerous
Merit Medical Systems, Inc. is voluntarily conducting a recall due to a potential discrepancy between the unit labeling of the Merit ReSolve Drainage Catheters and the actual device in the package.
The possibility exists for intraoperative reamer head breakages which could also allow for un-retrieved fragments of non-implant grade material: additional lot numbers identified. No new adverse events reported.
🏥 Medical Devices Class I - Dangerous
There are reports of post - operative inflammation and/or toxic anterior segment syndrome (TASS) after cataract surgery.
🏥 Medical Devices Class I - Dangerous
Complaints received of the front joint of the spring arm AC 2000 could break at the interface to the monitor.
🏥 Medical Devices Class I - Dangerous
Graduation marks of the syringe are not centered with the numeric position marks on the syringe barrel.
🏥 Medical Devices Class I - Dangerous
Certain lots of PT/INR cartridges may generate a higher than typical number of PT/INR star outs potentially delaying the generation of patient results for PT/INR.
Wall Chart for STERRAD 100NX System, P/N 10104. The STERRAD 100NX Sterilizer is designed for sterilization of both metal and nonmetal medical devices at low temperatures.
Advanced Sterilization Products
🏥 Medical Devices Class I - Dangerous
Advanced Sterilization PRoducts (ASP) is recalling the Wall Chart for STERRAD 100NX System because it incorrectly states "APTIMAX Instrument Trays can be enclosed in either polypropylene wrap or in Tyvek Pouches with STERRAD Chemical Indicators."
🏥 Medical Devices Class I - Dangerous
Graduation marks of the syringe are not centered with the numeric position marks on the syringe barrel.
🏥 Medical Devices Class I - Dangerous
AngioJet products were distributed with an incorrect use-by (expiry) date. The correct date is Nov-2015, but the units are labeled with a use-by date of Dec-2015.
Grizzly 10-inch hybrid table saws
Unknown Manufacturer
🏠 Consumer Products Class III - Low Risk
The motor pulley can come loose and hit the table saw blade, causing the blade teeth to break into flying metal fragments, posing a risk of laceration or impact injury to consumers.