Philips RS North America LLC (formerly Philips Respironics) has developed a plan to repair the polyester-based polyurethane foam in the recalled CPAP and BiPAP devices with a different, silicone-based foam. The FDA initially approved this plan based, in part, on testing the company provided to the FDA in June on the new foam. On Nov.…
Philips Reworking Recalled CPAP and BiPAP Devices with Silicone-Based Foam to Thwart Ozone & UV Problems
More from LegalMore posts in Legal »
- Vidul Prakash (Former CFO for Ultraviolet-Blocking Smart Glass Manufacturer View Inc.) Gets Access to Documents SEC Officials Wanted to Hide
- Judge Birotte Issues Mixed Expert Testimony Ruling in <i> Seoul Semiconductor v. FEIT Electric</i>
- Air Pros Solutions Files Chapter 11 Bankruptcy Petition in N.D. Ga., Intending to Sell Substantially All Assets
- Fishlock Plaintiffs Move for Class Certification & Global Plasma Moves for Summary Judgment
- Judge Brnovich Further Narrows Range of Dispute in <i>Lighting Defense v. Shanghai SANSI</i> LED Lighting Technology Patent Litigation & Parties Settle