- Recalling firm
- Medline Industries, LP
- Reason for recall
- Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
- Distribution pattern
- US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, FL, GA, IL, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, TN, TX, VA, WI, WY and the country of Barbados.
- State
- IL
- Status
- Ongoing
- Recall number
- Z-2583-2026
- Recall initiated
- February 27, 2026