ClearanceBrief
Recall Z-1515-2021 ยท BYI Percussor, Powered-Electric

Smiths Medical ASD Inc.

Palm Cups - Product Usage: intended to be used to percuss the chest wall to mobilize the secretions within the bronchial tree.

DateMar 31, 2021
StatusTerminated
ReasonThe firm became aware via complaints that one lot of ACE MDI Spacers with Small Masks and one lot of Palm Cups (Large) may have incorrect shipping box labels.
Root causeProcess control
ActionA Recall notification letter titled, "URGENT MEDICAL DEVICE FIELD SAFETY NOTICE" was sent to consignees beginning on 03/31/2021 via email. Consignees were notified to follow the instructions listed in the Recall Notice. Consignees were instructed to identify any affected devices in their possession (listed in the Recall Notice). If consignees have affected devices in their possession, the notice instructs them to inspect devices to determine if the device label matches the shipping box labels. The consignees should complete the response form and return to Smiths Medical. After the completed Fi
Quantity682 units
DistributionWorldwide distribution - US Nationwide distribution in the states of PA and MN. The countries of Columbia, Germany, Greece, Hong Kong, Qatar, Thailand, and United Arab Emirates.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K812166PERCUSSOR
Dhd Medical Products Div. Diemolding Corp., Aug 18, 1981