Z-1111-2026Class II

Tego Connector: REF: 011-D1000, 01C-D1000, 055-D1000, D1000; Conector Tego: REF: LAT-D1000

Name: Z-1111-2026 Tego Connector: REF: 011-D1000, 01C-D1000, 055-D1000, D1000; Conector Tego: REF: LAT-D1000
Creator: ICU Medical, Inc.
Published: 2025-12-19
License: https://open.fda.gov/license/

Abbott Medical / initiated 2025-12-19 / Open, Classified / root cause: manufacturing process

FDA source

ICU Medical, Inc. began a recall of Tego Connector: REF: 011-D1000, 01C-D1000, 055-D1000, D1000; Conector Tego: REF: LAT-D1000 on 2025-12-19. FDA classified it as Class II and gives the reason as "Needle free access device intended as accessory to vascular access used in hemodialysis or accessory to intravascular administration sets has a silicone seal which may bulge at the top, separate from the body, tear; may...". As of 2026-09-10, the recall status on record is Open, Classified, and MDM tags the root cause as manufacturing process.

Recall record

Recall number: Z-1111-2026
Classification: Class II
Status: Open, Classified
Initiated: 2025-12-19
Posted: 2026-01-16
Recalling firm: Abbott Medical
Product: Tego Connector: REF: 011-D1000, 01C-D1000, 055-D1000, D1000; Conector Tego: REF: LAT-D1000
Product code: FPA Set, Administration, Intravascular
Reason for recall: Needle free access device intended as accessory to vascular access used in hemodialysis or accessory to intravascular administration sets has a silicone seal which may bulge at the top, separate from the body, tear; may result in fluid leaks, occluded fluid flow, inability to inject/withdraw blood product, delayed/interrupted therapy, exposure to biological contaminants, air infused into the body
Root cause tag: manufacturing process
FDA root cause: Process control
Action: On 12/19/2025, correction notices were emailed to customers who were asked to do the following: 1) Destroy all affected products following your institution's process for destruction. If destroying is not immediately possible at your facility, then the product should be quarantined until disposal. 2) Share this notification with all potential users of the device, to ensure they are aware of this notification. If the devices are used at another location, please ensure this communication is delivered there. 3) Complete and return the Customer Response Form via email to [email protected] For further inquiries, please contact the firm: Global Complaint Management: [email protected] 1-(866)-216-8806; Customer Service: [email protected], 1-(800)-258-5361
Quantity in commerce: 14,684,607 items
Distribution: Worldwide - US Nationwide distribution including in the states of FL, AZ, RI, TN, KS, NJ, NY, VA, SC, GA, CA, MS, TX, OH, NC, MA, WA, IL, PA, NV, NH, LA, MI, NE, ME, MN, NM, OK, MD, IA, OR, SD, WI, MO, AL, WY, IN, KY, DC, UT, AR, WV, AK, ND, CO and the countries of BE, DE, CO, ES, AU, AR, SA, SI, IT, LK, MY, AT, FI, GB, TW, MX, NL, IE, CA, GR, ZA, SE, SK, NZ, LT, CH, HR, FR, JO, PE, SG, BR, PL, RO, HU, CZ, NO, AE, EE, CN, MA, HK.
Product codes and lots: UDI-DI: 00840619026059, 00840619006785. REF/Lot(Expiration): 011-D1000/14015455(5/1/2029), 14044313(6/1/2029), 14228823(12/1/2029), 14274294(1/1/2030); 01C-D1000/14171414(10/1/2029), 14304670(2/1/2030); 055-D1000/13772668(9/1/2028), 13778926(9/1/2028), 13791786(10/1/2028), 13794986(10/1/2028), 13797963(10/1/2028), 13801102(10/1/2028), 13806764(10/1/2028), 13812991(11/1/2028), 13822705(11/1/2028), 13828556(11/1/2028), 13833879(11/1/2028), 13838937(12/1/2028), 13867515(1/1/2029), 13875052(1/1/2029), 13876502(1/1/2029), 13876503(1/1/2029), 13882254(1/1/2029), 13882256(1/1/2029), 13887995(1/1/2029), 13887996(1/1/2029), 13894349(2/1/2029), 13894350(2/1/2029), 13903971(2/1/2029), 13903972(2/1/2029), 14045054(6/1/2029), 14045055(6/1/2029), 14049379(6/1/2029), 14049404(6/1/2029), 14063784(6/1/2029), 14063785(6/1/2029), 14071890(7/1/2029), 14071891(7/1/2029), 14071892(7/1/2029), 14087320(7/1/2029), 14090798(7/1/2029), 14110500(8/1/2029), 14131560(8/1/2029), 14144999(9/1/2029), 14145000(9/1/2029), 14150873(9/1/2029), 14150874(9/1/2029), 14150875(9/1/2029), 14170224(10/1/2029), 14170226(10/1/2029), 14179702(10/1/2029), 14179704(10/1/2029), 14179706(10/1/2029), 14208522(11/1/2029), 14208523(11/1/2029), 14212866(11/1/2029), 14212870(11/1/2029), 14216154(11/1/2029), 14216155(11/1/2029), 14224623(11/1/2029), 14248560(12/1/2029), 14248561(12/1/2029), 14274291(1/1/2030), 1427429291/1/2030), 14278257(1/1/2030), 14278258(1/1/2030), 14278259(1/1/2030), 14278260(1/1/2030), 14300970(2/1/2030), 14300972(2/1/2030), 14303936(2/1/2030); D1000/13768000(9/1/2028), 13772666(9/1/2028), 13778922(9/1/2028), 13778923(9/1/2028), 13778925(9/1/2028), 13791783(10/1/2028), 13791784(10/1/2028), 13791785(10/1/2028), 13792328(10/1/2028), 13794980(10/1/2028), 13794982(10/1/2028), 13794984(10/1/2028), 13801099(10/1/2028), 13801100(10/1/2028), 13801101(10/1/2028), 13806761(10/1/2028), 13806762(10/1/2028), 13806763(10/1/2028), 13812988(11/1/2028), 13812989(11/1/2028), 13812990(11/1/2028), 13822693(11/1/2028), 13822697(11/1/2028), 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14244970(12/1/2029), 14244971(12/1/2029), 1424497(12/1/2029), 14244977(12/1/2029), 14244978(12/1/2029), 14244980(12/1/2029), 14251976(12/1/2029), 14251977(12/1/2029), 14251979(12/1/2029), 14251980(12/1/2029), 14251983(12/1/2029), 14251984(12/1/2029), 14251985(1/1/2030), 14251986(12/1/2029), 14265939(1/1/2030), 14265940(1/1/2030), 14265941(1/1/2030), 14265942(1/1/2030), 14265943(1/1/2030), 14289207(1/1/2030), 14292935(2/1/2030), 14292936(2/1/2030), 14300977(2/1/2030), 14300979(2/1/2030), 14307683(2/1/2030), 14307684(2/1/2030), 14307685(2/1/2030); LAT-D1000/13768003(9/1/2028), 13778927(10/1/2028), 13812992(11/1/2028), 13848447(12/1/2028), 13867516(1/1/2029), 14015450(5/1/2029), 14044312(6/1/2029), 14063789(6/1/2029), 14090799(7/1/2029), 14145002(9/1/2029), 14228820(12/1/2029), 14228821(12/1/2029), 14228822(12/1/2029), 14274293(1/1/2030), 14274302(1/1/2030), 14307682(2/1/2030)

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-1111-2026
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-1111-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-01-28	2026-01-16

Product code FPA

K053106Class IITego, Model D1000Icu Medical, Inc. / cleared 2006-01-10

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 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)