Z-0770-2019 Class II Terminated

Recalled by LivaNova USA — Arvada, CO

FDA device recall Z-0770-2019 was initiated by LivaNova USA on Nov 9, 2018 and is designated Class II. Reason for recall: 4-way stopcocks and stopcock manifold assembled in certain perfusion tubing systems, indicated for use in surgical procedures requiring extracorporeal support for periods of up to six hours, may leak… The recall status is terminated (terminated May 3, 2022). Affected quantity: 483.

Recall Details

Product Type
Devices
Report Date
Jan 30, 2019
Initiation Date
Nov 9, 2018
Termination Date
May 3, 2022
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
483

Product Description

Perfusion Pack, Rx only, Sterile EO

Reason for Recall

4-way stopcocks and stopcock manifold assembled in certain perfusion tubing systems, indicated for use in surgical procedures requiring extracorporeal support for periods of up to six hours, may leak or be occluded.

Distribution Pattern

Worldwide Distribution - Domestic (US) Consignees: AR, AZ, CA, CO, CT, FL, GA, HI, IL, IN, KS, KY, LA, MA, MD, ME, MI, MO, NC, NE, NH, NJ, NM, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, VA, WA, WI, WV, MS; Foreign (OUS) Consignees: Canada

Code Information

Lot Numbers: 1819000027, 1813500044, 1809300053, 1817900004, 1821900089, 1812100018, 1816200009, 1817600016, 1810600004, 1811400014, 1812000017, 1812700017, 1813500013, 1815500011, 1816400023, 1809400005, 1811600025, 1812000018, 1812700018, 1813500014, 1814100012, 1815800010, 1810600006, 1811300003, 1812000019, 1812700020, 1815500012, 1817600017, 1813400007, 1814200096, 1816200011, 1817100013, 1813600009, 1817100103, 1819100014, 1810600014, 1812000030, 1815600027, 1817200017, 1819100017, 1810600015, 1816300051, 1815800015, 1817800028, 1810100021, 1810800022, 1811500019, 1812200022, 1813500020, 1814400026, 1815800017, 1816500016, 1817900015, 1810000025, 1810800023, 1811400022, 1812200023, 1813400010, 1814100019, 1816300053, 1810100022, 1812000034, 1812700032, 1814400027, 1816400032, 1817800031, 1819200020, 1812700034, 1814900020, 1817600031, 1814300026, 1818400082, 1819700023, 1820400020, 1814100022, 1816400035, 1818600024, 1811000017, 1815100030, 1816400036, 1819000012, 1809500011, 1810700016, 1812000036, 1814100023, 1815800018, 1810200011, 1814900021, 1817900017, 1806000020, 1807200053, 1810700018, 1811300015, 1812700035, 1816400037, 1819000013, 1810000027, 1812800072, 1814900022, 1813700002, 1817700022, 1819200022, 1810100026, 1811400028, 1803900021, 1805300025, 1805900033, 1806600023, 1807100016, 1810700020, 1811500023, 1813700014, 1814400028, 1816200018, 1817200020, 1811600032, 1814900023, 1816500019, 1817900019, 1812800073, 1815800019, 1819000016, 1810600022, 1813600016, 1818300026, 1810200014, 1812200029, 1814200103, 1815600031, 1816400039, 1818400085, 1821100028, 1810600023, 1810900022, 1813000021, 1817900021, 1803600019, 1803800017, 1805900035, 1806100020, 1806700039, 1807400038, 1808600021, 1812900030, 1813000022, 1806600064, 1814400031, 1816500022, 1818300027, 1817200022, 1810800024, 1812300012, 1804500029, 1806000024, 1810600024, 1812300013, 1818300028, 1810800025, 1812300014, 1813600019, 1819100023, 1811400001, 1811300019, 1811600034, 1812200032, 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Source

Dataset
openFDA device recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for Z-0770-2019
openFDA file date
Oct 21, 2026
Loaded by RegDataLab
Oct 23, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.