ClearanceBrief
Recall Z-2602-2023 ยท LZN Cement Obturator

Stryker Corporation

Stryker ACM (Advanced Cement Mixing)System: ACM Kit w/ Femoral Breakaway Nozzle, Restrictors & Prox. Med. Press- Allows the user to mix bone cement with a constant high vacuum through the process. Catalog Number: 0306-705-000

DateSep 19, 2023 (initiated Aug 7, 2023)
StatusOpen, Classified
ReasonPotential for the Break-Away Femoral Nozzle the applicator tip connecting the cement cartridge, to disassemble or break off during use, can lead to the potential for loss of function of the ACM system and bio-incompatibility due to components falling into surgical site
Root causeUnder Investigation by firm
ActionStryker issued Urgent Medical Device Recall letter on 8/07/23. Letter states reason for recall, health risk and action to take: Actions needed 1. Immediately review your inventory to locate and quarantine any affected products at your facility. 2. Return the enclosed Business Reply Form (BRF), even if affected product is no longer in inventory, to the email Instruments.Recalls@stryker.com. 3. Upon receipt of the completed BRF, Stryker will provide a shipping label to return recalled product on-hand. 4. A replacement order will be shipped to customers upon receipt of the recalled product. 5. Ma
Quantity231 units US; 21 units OUS
DistributionNationwide Foreign: Austria Belgium Canada France Germany Hong Kong Italy Malaysia Poland Singapore South Korea Spain Taiwan Thailand UK
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K931847BIO-PREP CEMENT RESTRICTOR
Biomedical Devices, Inc., Jun 28, 1994