Class II Recall

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

Summary

The FDA issued a Class II for Tego Connector: REF: 011-D1000, 01C-D1000, 055-D1000, D1000; Conector Tego: REF: by ICU Medical, Inc.. Reason: Needle free access device intended as accessory to vascular access used in hemodialysis or accessory to intravascular administration sets has a silico.

Details

Source

Device Recall

External ID

Z-1111-2026

Action Date

2026-01-28

Status

Ongoing

Product Description

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

Lot/Code Info: 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), 13822701(11/1/2028), 13825588(11/1/2028), 13828548(11/1/2028), 13828551(11/1/2028), 13828553(11/1/2028), 13833876(11/1/2028), 13833877(11/1/2028), 13833878(11/1/2028), 13838931(11/1/2028), 13838933(12/1/2028), 13838935(11/1/2028), 13848442(12/1/2028), 13848444(12/1/2028), 13848445(12/1/2028), 13854647(12/1/2028), 13854648(12/1/2028), 13854649(12/1/2028), 13858987(12/1/2028), 13859857(12/1/2028), 13859858(12/1/2028), 13859859(12/1/2028), 13867512(1/1/2029), 13867514(1/1/2029), 13876507(1/1/2029), 13876508(1/1/2029), 13876509(1/1/2029), 13882259(1/1/2029), 13882260(1/1/2029), 13887205(1/1/2029), 13887206(1/1/2029), 13887997(1/1/2029), 13894351(1/1/2029), 13894352(2/1/2029), 13894353(2/1/2029), 13903974(2/1/2029), 13903975(2/1/2029), 13903976(2/1/2029), 13903977(2/1/2029), 13910270(2/1/2029), 13910272(2/1/2029), 13938363(3/1/2029), 13938364(3/1/2029), 13938366(3/1/2029), 13943704(3/1/2029), 13943708(3/1/2029), 13943712(3/1/2029), 13943720(3/1/2029), 13949234(3/1/2029), 13953949(3/1/2029), 13953954(4/1/2029), 13953956(4/1/2029), 13953958(4/1/2029), 13955847(4/1/2029), 13959937(4/1/2029), 13959944(4/1/2029), 13959950(4/1/2029), 13959956(4/1/2029), 13971720(4/1/2029), 13971744(4/1/2029), 13971752(4/1/2029), 13971761(4/1/2029), 13971773(4/1/2029), 13979279(4/1/2029), 13979290(4/1/2029), 13979293(4/1/2029), 13979298(4/1/2029), 13979303(4/1/2029), 13979306(4/1/2029), 13979308(4/1/2029), 13982887(4/1/2029), 13982888(4/1/2029), 13986330(4/1/2029), 13986339(4/1/2029), 13986376(5/1/2029), 13986393(4/1/2029), 13986399(4/1/2029),13986406(4/1/2029), 13986440(4/1/2029), 13999996(5/1/2029), 13999997(5/1/2029), 13999999(5/1/2029), 14000000(5/1/2029), 14000001(5/1/2029), 14000002(5/1/2029), 14000003(5/1/2029), 14015459(5/1/2029), 14015462(5/1/2029), 14015463(5/1/2029), 14015464(5/1/2029), 14015467(5/1/2029), 14021608(5/1/2029), 14021610(5/1/2029), 14021611(5/1/2029), 14021612(5/1/2029), 14021613(5/1/2029), 14027546(5/1/2029), 14027547(5/1/2029), 14027548(5/1/2029), 14027549(5/1/2029), 14027551(5/1/2029), 14027552(5/1/2029), 14027553(5/1/2029), 14036497(5/1/2029), 14036498(5/1/2029), 14036499(5/1/2029, 14036500(6/1/2029), 14036501(6/1/2029), 14036502(6/1/2029), 14036503(6/1/2029), 14037604(6/1/2029), 14037605(6/1/2029), 14041790(6/1/2029), 14041792(6/1/2029), 14041793(6/1/2029), 14041795(6/1/2029), 14041797(6/1/2029), 14041798(6/1/2029), 14041800(6/1/2029), 14056392(6/1/2029), 14056393(6/1/2029), 14056395(6/1/2029), 14056397(6/1/2029), 14056398(6/1/2029), 14056399(6/1/2029), 14056400(6/1/2029), 14063790(6/1/2029), 14063791(7/1/2029), 14063792(7/1/2029), 14071894(7/1/2029), 14071895(7/1/2029), 14087321(7/1/2029), 14087322(7/1/2029), 14087323(7/1/2029), 14090800(7/1/2029), 14090801(8/1/2029), 14097661(8/1/2029), 14097662(8/1/2029), 14100193(8/1/2029), 14100198(8/1/2029), 14110501(8/1/2029), 14110502(8/1/2029), 14110503(8/1/2029), 14110505(8/1/2029), 14115072(8/1/2029), 14115073(8/1/2029), 14115074(8/1/2029), 14115075(8/1/2029), 14115076(8/1/2029), 14131561(8/1/2029), 14131562(9/1/2029), 14131563(9/1/2029), 14131564(9/1/2029), 14135720(9/1/2029), 14135721(9/1/2029), 14135722(9/1/2029), 14135723(9/1/2029), 14135725(9/1/2029), 14145003(9/1/2029), 14145004(9/1/2029), 14145005(9/1/2029), 14147959(9/1/2029), 14150877(9/1/2029), 14150878(10/1/2029), 14150880(9/1/2029), 14162155(10/1/2029), 14170227(10/1/2029), 14170231(10/1/2029), 14170232(10/1/2029), 14179721(10/1/2029), 14183938(10/1/2029), 14183940(10/1/2029), 14183941(10/1/2029), 14192702(10/1/2029), 14192703(10/1/2029), 14201160(11/1/2029), 14201161(11/1/2029), 14201162(11/1/2029), 14201163(11/1/2029), 14201165(11/1/2029), 14216156(11/1/2029), 14216157(11/1/2029), 14219693(11/1/2029), 14219694(11/1/2029), 14224627(11/1/2029), 14224630(11/1/2029), 14226006(11/1/2029), 14226007(11/1/2029), 14226008(11/1/2029), 14226009(11/1/2029), 14226010(11/1/2029), 14226011(12/1/2029), 14226012(12/1/2029), 14226013(12/1/2029), 14228825(12/1/2029), 14228826(12/1/2029), 14228828(12/1/2029), 14228832(12/1/2029), 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)

Quantity Affected: 14,684,607 items

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

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.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-12-19

Company

ICU Medical, Inc.

San Clemente, CA

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 180 device recalls issued in the same week, part of 413 device-related FDA actions this month.

ICU Medical, Inc. has 95 FDA actions in our database, including 85 recalls and 10 clearances.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (ICU Medical, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does ICU Medical, Inc. have FDA actions?

ICU Medical, Inc. has 95 FDA actions in our database, including 85 recalls and 10 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "Z-1111-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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