Abbott Vascular: Medical Device Recall in 2022 - (Recall #: Z-0924-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

INDEFLATOR Plus 30 - REF 1000183 WPL2122277-01 (2019-03-01)

Product Classification:

Class II

Date Initiated: March 11, 2022

Date Posted: April 20, 2022

Recall Number: Z-0924-2022

Event ID: 89760

Reason for Recall:

Due to an increase in complaint trend for leaks and intermittent/loose connections.

Status: Ongoing

Product Quantity: 6 lots

Code Information:

Part Numbers: 1000183 Device Identifier-GTIN: 08717648013584 Lot Numbers: 60316775 60322179 60328352 60322176 60326322 60337153

Distribution Pattern:

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, Saudi Arabia, Canada, India, Singapore, Switzerland, Italy, Slovakia, Chile, Jamaica, Thailand, China, Japan, Taiwan Republic of China, Colombia, Korea (South), Costa Rica, Luxembourg, Uruguay, Czech Republic, Mexico, Vietnam, Germany, Netherlands, South Africa, Dominican Republic, New Zealand, Spain, and Panama

Voluntary or Mandated:

Voluntary: Firm initiated