Philips North America recalls Model Number: 712010.
- Recalling company
- Philips North America
- Product
- Model Number: 712010.
- Reason
- Potential for the device to fail immediately after an exposure, causing the system to remain stationary.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Sep 18, 2026
- Reported
- Nov 4, 2026
- Distribution
- Worldwide Distribution: (US Nationwide) and International distribution to Angola, Australia, Austria, Canada, Chile, Cook Islands, Finland, France, Germany, Ghana, Gibraltar, Guadeloupe, Honduras, Israel, Italy, Latvia, Lithuania, Macedonia, Namibia, Netherlands, New Zealand, Poland, Portugal, Romania, Saudi Arabia, Singapore, Slovenia, South Africa, Spain, Switzerland, United Arab Emirates, United Kingdom.
- Status
- Ongoing
- Quantity
- 563 units
- Lot / codes
- Model Number: 712010. UDI: (01)00884838115521(21)26000155, (01)00884838115521(21)26000154, (01)00884838115521(21)26000151, (01)00884838115521(21)26000150, (01)00884838115521(21)26000149, (01)00884838115521(21)26000148, (01)00884838115521(21)26000147, (01)00884838115521(21)26000146, (01)00884838115521(21)26000145, (01)00884838115521(21)26000144, (01)00884838115521(21)26000143, (01)00884838115521(21)26000142, (01)00884838115521(21)26000141, (01)00884838115521(21)26000140, (01)00884838115521(21)26000139, (01)00884838115521(21)26000138, (01)00884838115521(21)26000137, (01)00884838115521(21)26000136, (01)00884838115521(21)26000135, (01)00884838115521(21)26000134, (01)00884838115521(21)26000133, (01)00884838115521(21)26000132, (01)00884838115521(21)26000129, (01)00884838115521(21)26000125, (01)00884838115521(21)26000126, (01)00884838115521(21)26000131, (01)00884838115521(21)26000130, (01)00884838115521(21)26000124, (01)00884838115521(21)26000123, (01)00884838115521(21)26000122, (01)00884838115521(21)26000121, (01)00884838115521(21)26000120, (01)00884838115521(21)26000119, (01)00884838115521(21)26000118, (01)00884838115521(21)26000116, (01)00884838115521(21)26000115, (01)00884838115521(21)26000113, (01)00884838115521(21)26000110, (01)00884838115521(21)26000109, (01)00884838115521(21)26000108, (01)00884838115521(21)26000107, (01)00884838115521(21)26000106, (01)00884838115521(21)26000117, (01)00884838115521(21)26000114, (01)00884838115521(21)26000111, (01)00884838115521(21)26000112, (
- Company location
- Cambridge, MA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-0288-2027
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-0288-2027 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.