FDA Device recall Z-1821-2015

Sure T, contact, contact detach, neria, neria detach, neria multi and thalaset Used in combination with infusion pumps for continuous subcu…

FDA Device
Class II
terminated
Published 2015-07-01

On 2015-07-01 the FDA classified a Class II recall of Sure T, contact, contact detach, neria, neria detach, neria multi and thalaset Used in combination with infusion pumps for continuous subcu… by Unomedical As, citing unomedical has found that in rare cases the steel needle can break during use, interrupting the delivery of medication including insulin.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-1821-2015
Classification	Class II
Status	terminated
Initiated	2015-05-21
Published	2015-07-01
Last updated	2026-09-13 11:53 UTC
Company	Unomedical As
Distribution	CA, IL, MN, PA

Product

Sure T, contact, contact detach, neria, neria detach, neria multi and thalaset Used in combination with infusion pumps for continuous subcutaneous infusion of medication.

Reason

Unomedical has found that in rare cases the steel needle can break during use, interrupting the delivery of medication including insulin.

Identifiers

code_info	210131, 212482, 213575, 213576, 214509, 214511, 216175, 216295, 216296, 218110, 218111, 218685, 219030, 219075, 220160,… 210131, 212482, 213575, 213576, 214509, 214511, 216175, 216295, 216296, 218110, 218111, 218685, 219030, 219075, 220160, 220161, 220163, 223771, 224282, 224283, 224284, 224285, 224286, 226935, 226939, 226940, 227062, 227063, 227064, 227065, 227892, 227894, 229302, 230245, 231124, 231127, 231130, 232701, 232702, 233875, 656782, 656785, 657341, 657836, 657966, 667536, 669845, 4262911, 4263093, 4263094, 4263095, 4263098, 4263099, 4263100, 4263112, 4263113, 4263130, 4263131, 4263132, 4263170, 4263171, 4263172, 4263178, 4263179, 4263293, 4263240, 4263241, 4263307, 4263308, 4263328, 4263329, 4263372, 4263391, 4263393, 4263394, 4263400, 4263420, 4263421, 4263458, 4263474, 4263475, 4263476, 4263486, 4263517, 4263529, 4263551, 4263552, 4263571, 4263572, 4263580, 4263609, 4263624, 4263631, 4263665, 4263677, 4263678, 4263694, 4263695, 4263696, 4263716, 4263718, 4263719, 4263738, 4263750, 4263778, 5000119, 5000120, 5001718, 5003702, 5003920, 5003921, 5006040, 5006041, 5006567, 5006568, 5006571, 50

code_info

210131, 212482, 213575, 213576, 214509, 214511, 216175, 216295, 216296, 218110, 218111, 218685, 219030, 219075, 220160,…

210131, 212482, 213575, 213576, 214509, 214511, 216175, 216295, 216296, 218110, 218111, 218685, 219030, 219075, 220160, 220161, 220163, 223771, 224282, 224283, 224284, 224285, 224286, 226935, 226939, 226940, 227062, 227063, 227064, 227065, 227892, 227894, 229302, 230245, 231124, 231127, 231130, 232701, 232702, 233875, 656782, 656785, 657341, 657836, 657966, 667536, 669845, 4262911, 4263093, 4263094, 4263095, 4263098, 4263099, 4263100, 4263112, 4263113, 4263130, 4263131, 4263132, 4263170, 4263171, 4263172, 4263178, 4263179, 4263293, 4263240, 4263241, 4263307, 4263308, 4263328, 4263329, 4263372, 4263391, 4263393, 4263394, 4263400, 4263420, 4263421, 4263458, 4263474, 4263475, 4263476, 4263486, 4263517, 4263529, 4263551, 4263552, 4263571, 4263572, 4263580, 4263609, 4263624, 4263631, 4263665, 4263677, 4263678, 4263694, 4263695, 4263696, 4263716, 4263718, 4263719, 4263738, 4263750, 4263778, 5000119, 5000120, 5001718, 5003702, 5003920, 5003921, 5006040, 5006041, 5006567, 5006568, 5006571, 50

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1821-2015%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.