Innovative Orthopedic Technologies, LLC recalls ARCH Leg Positioning System
Due to the holes not being bored to the specific diameter, the locking pins are unable to engage under a load.
Read the official notice →- Date
- 2021-10-13
- Country
- United States
- Brand
- Innovative Orthopedic Technologies, LLC
- Product
- ARCH Leg Positioning System
- Classification
- Class II
- Units
- U.S. Nationwide distribution in the states of AL, AZ, FL, MI, MN, OK, SD, and…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
Other drugs & medical recalls in the United States
- 2021-10-13
USDatascope Corp. recalls Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), Model Nos. 0998-00-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-00-0800-34,…
The Helium Indicator on the Cardiosave display may over represent the amount of helium in unit in the presence of Electromagnetic Interference.
- US
DePuy Orthopaedics, Inc. recalls ATTUNE Revision Tibial Augment Size 7/8 5mm- intended for knee joint replacement Part Code:152307001
Packaging may include screws that are not intended to be used with the 5mm augments, may cause delay in surgery
FDA · DeviceDePuy Orthopaedics, Inc.US Nationwide distribution in the states of CA, LA, MN, MO, NC, NE, OR, PA,…Official notice → - US
Angiodynamics, Inc. recalls AngioDynamics NanoKnife Disposable Single Electrode Probes, Irreversible Electroporation (IRE) Device, 15 cm IRE Single Electrode RFID…
Programming issue affected RFID function of a single lot and did not allow the NanoKnife probes to be recognized by the NanoKnife generator.
FDA · DeviceAngiodynamics, Inc.Internationally distribution to the countries of Australia, Germany, Denmark,…Official notice → - US
Philips Ultrasound Inc recalls Philips Ultrasound, Inc. Sparq, Diagnostic Ultrasound System, REF 795116, 100-240V -, 50/60 Hz, 500 VA, CE2797, Rx Only,
Battery system data issue with the ultrasound system can intermittently cause a system shutdown, regardless of actual battery state or application of alternating current power.
FDA · DevicePhilips Ultrasound IncWorldwide distribution - US Nationwide distribution in the states of CA, MA,…Official notice → - US
CardioQuip, LLC recalls CardioQuip, Modular Cooler-Heater 1000(i), Refrigeration Module, Model: MCH-10RMS, UDI: (01)00860000846127 used with heat exchange devices.
There is the potential bacterial including Nontuberculous mycobacterial (NTM) to grow in the water system of heater-cooler devices which could result in contaminated water potentially aerosolized into the operating…
FDA · DeviceCardioQuip, LLCWorldwide distribution - US Nationwide distribution including in the states of…Official notice → - US
ZOLL Circulation, Inc. recalls ZOLL, REF 8700-0793-40 (SL-2593AE) SOLEX 7, Intravascular Heat Exchange Catheter Kit with central venous infusion capabilities (3 lumens),…
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
FDA · DeviceZOLL Circulation, Inc.Worldwide distribution - US Nationwide distribution in the states of AL, AZ,…Official notice →