Z-1056-2026Class II

Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) IV START...

Name: Z-1056-2026 Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) IV START...
Creator: Medline Industries, LP
Published: 2025-11-26
License: https://open.fda.gov/license/

MEDLINE INDUSTRIES, LP - Northfield / initiated 2025-11-26 / Open, Classified / root cause: manufacturing process

FDA source

Medline Industries, LP began a recall of Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) IV START KIT NS, Medline kit SKU DYKM1980C; 2) (134) L&D... on 2025-11-26. FDA classified it as Class II and gives the reason as "Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed...". 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-1056-2026
Classification: Class II
Status: Open, Classified
Initiated: 2025-11-26
Posted: 2026-01-12
Recalling firm: MEDLINE INDUSTRIES, LP - Northfield
Product: Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) IV START KIT NS, Medline kit SKU DYKM1980C; 2) (134) L&D IV-START SET, Medline kit SKU DYKM2137B; 3) IV START KIT, Medline kit SKU DYKS1372C; 4) IV START KIT, Medline kit SKU DYNDV1691B; 5) OUTPATIENT 2 TO 5 YEARS, Medline kit SKU DYNDV2464A.
Product code: LRS I.V. Start Kit
Reason for recall: Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.
Root cause tag: manufacturing process
FDA root cause: Nonconforming Material/Component
Action: Medline issued an URGENT MEDICAL DEVICE CORRECTION notice to its consignees on 11/26/2025 via email and USPS first class mail. The notice explained the issue potential risk to the patient, and referred the consignee to the attached B Braun notice for further instructions. The B Braun notice provide "Interim Measures for Users" to provide for the continued use of the product. For questions, contact the Recall Department at 866-359-1704 or [email protected].
Quantity in commerce: 5314 units
Distribution: US Nationwide distribution.
Product codes and lots: Medline kit SKU DYKM1980C, UDI/DI 10195327608309 (EA) 40195327608300 (CS), Lot Number 25JBB147; Medline kit SKU DYKM1980C, UDI/DI 10195327608309 (EA) 40195327608300 (CS), Lot Number 25KBL305; Medline kit SKU DYKM2137B, UDI/DI 10198459285615 (EA) 40198459285616 (CS), Lot Number 25HBT834; Medline kit SKU DYKM2137B, UDI/DI 10198459285615 (EA) 40198459285616 (CS), Lot Number 25IBJ757; Medline kit SKU DYKM2137B, UDI/DI 10198459285615 (EA) 40198459285616 (CS), Lot Number 25JBJ557; Medline kit SKU DYKS1372C, UDI/DI 10195327373504 (EA) 40195327373505 (CS), Lot Number 25JLA480; Medline kit SKU DYNDV1691B, UDI/DI 10195327658472 (EA) 40195327658473 (CS), Lot Number 25HBI335; Medline kit SKU DYNDV1691B, UDI/DI 10195327658472 (EA) 40195327658473 (CS), Lot Number 25IBE523; Medline kit SKU DYNDV1691B, UDI/DI 10195327658472 (EA) 40195327658473 (CS), Lot Number 25JBM702; Medline kit SKU DYNDV2464A, UDI/DI 10195327065911 (EA) 40195327065912 (CS), Lot Number 25IBV942.

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-1056-2026
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-1049-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-01-21	2026-01-12
Z-1050-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-01-21	2026-01-12
Z-1051-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-01-21	2026-01-12
Z-1052-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-01-21	2026-01-12
Z-1053-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-01-21	2026-01-12
Z-1054-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-01-21	2026-01-12
Z-1055-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-01-21	2026-01-12
Z-1056-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-01-21	2026-01-12
Z-1057-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-01-21	2026-01-12
Z-1058-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-01-21	2026-01-12
Z-1059-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-01-21	2026-01-12
Z-1060-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-01-21	2026-01-12

Product code LRS

The FDA recall record names no cleared device, and no clearance has been matched to it.

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)