PTW NORTH AMERICA CORPORATION recalls Software BeamAdjust version 2.2, Catalog No: S070009 Software VeriSoft version 8.0, Catalog No: S080032
When a measurement with a PTW detector array is performed with the software BeamAdjust 2.2 or VeriSoft 8.0, a measurement error can occur under specific conditions. This error can lead to a too-low or too-high measured…
Read the official notice →- Date
- 2022-01-19
- Country
- United States
- Brand
- PTW NORTH AMERICA CORPORATION
- Product
- Software BeamAdjust version 2.2, Catalog No: S070009 Software VeriSoft version 8.0, Catalog No: S080032
- Classification
- Class II
- Units
- US Nationwide distribution in the state of CO.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2022-01-19
USMedtronic Perfusion Systems recalls Medtronic Custom Perfusion kits, with the following product descriptions and corresponding model numbers: 1. CUSTOM PACK BB10Q85R…
Product is labeled as non-pyrogenic but endotoxin testing was not performed.
FDA · DeviceMedtronic Perfusion SystemsWorldwide distribution - US Nationwide distribution in the states of AL, AR,…Official notice →- US
DePuy Orthopaedics, Inc. recalls GLOBAL UNITE REV STEM SZ 10 Product Code: 110010600
Stems may have an undersized spigot bore diameter therefore separating the proximal body from the stem may not be possible without surgical delay and/or bone damage
FDA · DeviceDePuy Orthopaedics, Inc.Worldwide distribution - US Nationwide and the countries of Austria,…Official notice → - US
Ohio Medical Corporation recalls Instavac Portable Suction Pump, Constant mode (model #757000, Instavac C) and Intermittent mode (model 756000, Instavac I); and Instavac…
Increase in premature device failures
FDA · DeviceOhio Medical CorporationUS Nationwide, including PR. There was government and foreign distribution.…Official notice → - US
Haag-Streit USA Inc recalls OCT-Camera 211 01 A3; Running software iOCT-Control 3 v1.4
Malfunction of the automatic laser beam shut-off, the OCT unit might not recognize whether the laser beam is safely switched off
- US
Philips North America Llc recalls Wireless Footswtich used with the following Philips Allura Xper and Azurion Interventional Fluoroscopic X-ray System . Model Number:…
Wireless foot switch connection issues causing interruption of Fluoroscopy and exposure
FDA · DevicePhilips North America LlcWorldwide distribution - US Nationwide and the countries of Canada, Australia,…Official notice → - US
Siemens Medical Solutions USA, Inc recalls SOMATOM Edge Plus-Computed tomography system Model 1026700
Software version VB20_SP5 my lead to a relevant degradation of head image quality, a potential risk to patients is misdiagnosis.