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Recall Observatory FDA recall evidence

Device product

CS5/5+ Fastpacks, 125 mL, 150¿ Res Autotransfusion Device - Product Usage: its related accessory components are intended to be used for the recovery and processing of blood shed during or subsequent to an operation or as a result of trauma.

Z-0888-2020

October 21, 2019

Class II

Product summary

Firm
Haemonetics Corporation
Event
Event 84183
Status
Terminated
Classification
Class II
Quantity
14095
Official record key
device-enforcement:Z-0888-2020

Official wording

Reason: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell Saver¿ Elite¿/Elite¿ +125ml and 225ml bowl sets. Which could result in fluid being trapped inside the bowl core, causing a long empty device error message with the possibility of incomplete washing.

Code information: Catalog number/FG Item Number: 00265-00 1. Specific Lots with Bowl Cracks (720 distributed) Lot numbers: 1812011HTT 1902006HTT 1902007HTT 2. Missing instructions to check for cracks in IFU All products/lost manufactured between October 2014 and October 2019.

Distribution pattern: Worldwide distribution - US Nationwide distribution in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY, and countries of NZ, AU, IN, PK, PH, HK, VN, MY, ID, SG, CN, AT, DE, FR, GB, IT, CH.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell Saver¿ Elite¿/Elite¿ +125ml and 225ml bowl sets. Which could result in fluid being trapped inside the bowl core, causing a long empty device error message with the possibility of incomplete washing.