FDA recall Z-0325-2023

Busse Hospital Disposables, Inc. · Class II · device

Product

Busse JOINT INJECTION TRAY -Intended as a nerve block REF No. 8561 R1

Reason for recall

Kits containing 3M Steri-Drape Surgical Drapes recalled by 3M due to liner on the adhesive component is difficult to remove without damaging the product and may render the product unusable

Distribution

Key facts

Status: Ongoing
Initiation date: 2022-10-21
Report date: 2022-12-07
Voluntary/Mandated: Voluntary: Firm initiated
Location: Hauppauge, NY, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0325-2023