ClearanceBrief
Recall Z-2150-2018 ยท BTM Ventilator, Emergency, Manual (Resuscitator)

Sun Med, LLC

MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK, BAG RESERVOIR, PEEP VALVE, CO2 AND 7 FT. OXYGEN TUBING, REF CPRM1116PC

DateMay 24, 2018
StatusTerminated
ReasonThere is a potential for the patient port retaining ring to not fully seat allowing the patient port to detach during use. This may impact air delivery to the patient.
Root causeMixed-up of materials/components
ActionOn May 25, 2018 Sun Med, LLC issued URGENT MEDICAL DEVICE PRODUCT REMOVAL notices to two of their customers. On June 1, 2018 Sun Med, LLC issued a press release. Customers were encouraged to take the following actions: 1) Examine inventory, quarantine and cease distribution of impacted product. 2) If customers further distributed product, please identify your customers/consignees and notify them of this product removal. Your notification may be enhanced by including a copy of the removal notice. If you need any assistance contacting your customers, please inform SunMed. 3) Complete and ret
Quantity40 cases
DistributionIL & OH distributors
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K953546MANUAL PULMONARY RESUSICITATOR
Medical Marketing Concepts, Feb 29, 1996