Z-0770-2019Class II

Perfusion Pack, Rx only, Sterile EO

Name: Z-0770-2019 Perfusion Pack, Rx only, Sterile EO
Creator: LivaNova USA
Published: 2018-11-09
License: https://open.fda.gov/license/

LivaNova USA, Inc. / initiated 2018-11-09 / Terminated / root cause: manufacturing process

FDA source

LivaNova USA began a recall of Perfusion Pack, Rx only, Sterile EO on 2018-11-09. FDA classified it as Class II and gives the reason as "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". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as manufacturing process.

Recall record

Recall number: Z-0770-2019
Classification: Class II
Status: Terminated
Initiated: 2018-11-09
Posted: 2019-01-23
Terminated: 2022-05-03
Recalling firm: LivaNova USA, Inc.
Product: Perfusion Pack, Rx only, Sterile EO
Product code: DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
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.
Root cause tag: manufacturing process
FDA root cause: Process control
Action: On 11/09/2018 Medical Device Correction Notices were mailed to customers via UPS First Overnight. Customers were advised: 1) Inspect your stock and identify Perfusion Tubing System(s) belonging to the impacted lots in inventory, as noted in Attachment 1. 2) The recalling firm will be shipping one case of sterile stopcocks (part number: SCO4S) and manifolds (part number: 020581600) to your facility as an immediate replacement for those remaining that may be defective in your impacted Perfusion Tubing System stock. 3) As each affected pack is opened for use, please replace the original stopcocks in the pack with the spare provided by the firm. The original stopcocks should be destroyed/ discarded. 4) Contact your firm Representative if additional replacement stopcocks are required. In addition, customers were asked to complete and return the attached Customer Response Form. Also, to assure within their organization that the correction notice is communicated to all personnel who need to be aware of it. For questions about this Medical Device Correction, please contact (800) 986-4702 or e-mail [email protected]
Quantity in commerce: 483
Distribution: 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
Product codes and lots: 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, 1814400033, 1819000020, 1809400017, 1814900027, 1815600032, 1810600026, 1811600035, 1817700026, 1819200027, 1810100028, 1813400015, 1815800021, 1817600036, 1810200016, 1811400031, 1812700040, 1815500028, 1816200021, 1816500024, 1818600028, 1811500024, 1812900031, 1814400034, 1816900018, 1812900032, 1817100021, 1817800035, 1813000025, 1816300058, 1819200028, 1811400033, 1814200105, 1816900020, 1817900023, 1807800020, 1808100036, 1805200067, 1810100030, 1819200029, 1806000029, 1807400042, 1813400017, 1816200024, 1815000041, 1818600030, 1819100025, 1810800030, 1812300017, 1816200027, 1816400043, 1817000037, 1817600038, 1819300025, 1809300068, 1813600022, 1816400079, 1821100036, 1809500017, 1811500029, 1811600040, 1812200037, 1814300030, 1815100034, 1815800023, 1817000038, 1817700032, 1818600032, 1812100075, 1813400057, 1814200109, 1814300031, 1820600034, 1810600029, 1812900034, 1813500027, 1819000023, 1810800033, 1813000032, 1813700022, 1816500025, 1814400069, 1810600032, 1811500033, 1813400021, 1815100037, 1818400090, 1812900039, 1813500029, 1816500026, 1818600034, 1810800034, 1811300023, 1812000043, 1813700025, 1814900031, 1816200029, 1816500027, 1817000040, 1818300031, 1804600025, 1805800065, 1806600028, 1810100035, 1811600042, 1813500030, 1816200030, 1812200001, 1816400087, 1816400048, 1817600041, 1811000008, 1810800065, 1817100025, 1817600042, 1817900029, 1812000088, 1818600079, 1816400050, 1812900041, 1814100030, 1815800024, 1810100081, 1810700112, 1811300062, 1817600043, 1818300033, 1805200031, 1805900040, 1807200067, 1812100042, 1815000047, 1817100027, 1811500035, 1812800074, 1822100076, 1810900029, 1813000033, 1814200112, 1814900035, 1815600039, 1816400051, 1814100032, 1816900025, 1812200045, 1815600041, 1817000042, 1817900030, 1812000010, 1805200035, 1806600030, 1809500023, 1811400037, 1813600030, 1810000033, 1811600046, 1813000039, 1815100041, 1815800028, 1817100030, 1818400143, 1814900036, 1813600001, 1814100001, 1812300001, 1815100065, 1809500025, 1811400040, 1812200050, 1813500036, 1813700027, 1815800031, 1816500032, 1818600039, 1810600036, 1811500039, 1812900044, 1816200031, 1817000044, 1818400096, 1817700085, 1818600075, 1809900043, 1811600049, 1817700038, 1818600040, 1807100026, 1807800034, 1810000035, 1812300023, 1810700030, 1809900044, 1812200051, 1819000029, 1819200036, 1810600037, 1811500042, 1812200052, 1814900040, 1816200033, 1817800043, 1815800033, 1821200047, 1809500028, 1812000047, 1809900048, 1810800040, 1813500041, 1815500034, 1817700039, 1816500033, 1805100104, 1806400043, 1807400052, 1809500030, 1812100053, 1813500042, 1818400097, 1810200032, 1815600050, 1816500036, 1810800043, 1813400028, 1818300039, 1818400098, 1815600051, 1810800044, 1818300040, 1810200033, 1812300026, 1815100046, 1817800070, 1818600042, 1810100043, 1817200037, 1812000050, 1812300029, 1816300076, 1817700042, 1810100044, 1810700034, 1811400048, 1812300030, 1813700031, 1817200038, 1807100034, 1803700065, 1806400048, 1807100035, 1808500045, 1810800045, 1812000051, 1814300043, 1815700038, 1817700043, 1818600044, 1803700066, 1805200043, 1811400062, 1813400034, 1813700032, 1810700038, 1803600044, 1806100041, 1807100040, 1808800042, 1812300032, 1813600036, 1816200040, 1817900042, 1810800046, 1811500052, 1812800085, 1813600037, 1818600047, 1803700072, 1811600060, 1812700059, 1815800045, 1819100045, 1813600039, 1815800046, 1817800051, 1808600043, 1803600047, 1803700075, 1811000043, 1812700061, 1814400048, 1817800052, 1809500037, 1811000044, 1815500042, 1816400064, 1818600051, 1810000045, 1812000062, 1811300042, 1811600066, 1815500045, 1819000047, 1816400068, 1817100047, 1819100050, 1809500040, 1811600067, 1813500049, 1815000056, 1817800054, 1812000002, 1813700038, 1815800050, 1806400055, 1808500048, 1806600059, 1819000051, 1817800055, 1813400049, 1819000054

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-0770-2019
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-0770-2019	Class II	Terminated	Voluntary: Firm initiated	2019-01-30	2019-01-23

Product code DWF

K881330Class IICobe Heart/lung Perfusion and Cardioplegia PackCobe Laboratories, Inc. / cleared 1988-06-10

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-10-07, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)