INDEFLATOR Plus 30 - REF 1000183 WPL2122277-01 (2019-03-01)
Check against the official notice below — it lists the full affected range.
Abbott Vascular is recalling INDEFLATOR Plus 30 devices (model REF 1000183) due to an increase in complaints about leaks and intermittent or loose connections. The recall affects six specific lot numbers: 60316775, 60322179, 60328352, 60322176, 60326322, and 60337153. The affected devices were distributed nationwide across the United States, Puerto Rico, and multiple international locations including the United Kingdom, France, Australia, Brazil, and others.
The recall record does not specify a remedy or corrective action for affected consumers.
Written by software from the official notice below. Not reviewed by a lawyer.
Due to an increase in complaint trend for leaks and intermittent/loose connections.
Reason for recall: Due to an increase in complaint trend for leaks and intermittent/loose connections. Distribution: U.S Nationwide Distribution.: AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, Puerto Rico, SC, TN, TX, VA, WA, and WI. O.U.S.: United Arab Emirates, France, Pakistan, Argentina, United Kingdom, Portugal, Australia, Greece, R¿union, Belgium, Guam, Romania, Brazil, Indonesia, Russian Federation, Bahamas, Israel, Quantity: 6 lots Lot/code info: Part Numbers: 1000183 Device Identifier-GTIN: 08717648013584 Lot Numbers: 60316775 60322179 60328352 60322176 60326322 60337153
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.