Erbe Medical, LLC recalls ERBEFLO 2, Endoscopy Pump Tubing/Cap Set, REF: 20325-222

Recall date

March 31, 2026

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2064-2026

FDA classification

Class II

Brand / firm

Erbe Medical, LLC

Sold / distributed

US Nationwide distribution including in the states of IL, NY, CA, WA, UT, KY, PA, TX, AL, OH, FL, IN, NJ, NH, MI, CT, AR, MN, WI, AZ, CO, WV, MT, HI, TN, GA, VA, OK, RI, MO, NM, ID, SC, WY, KS, NC, MS, OR, MD, MA, DE, NE, AK, IA, DC, ME, LA, SD, ND, VT, PR, NV.

Why it was recalled

Devices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible to unintended water flow from distal tip under unsupported third-party connector use conditions, which may lead to water aspiration, which may progress to aspiration pneumonia, acute respiratory distress syndrome, or respiratory failure.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

ERBEFLO 2, Endoscopy Pump Tubing/Cap Set, REF: 20325-222