CLASS I ONGOING Device recall · Reported 1 Jul 2026 · FDA Enforcement Report

Medline Convenience Kits: Drawer 6 Central Line Insertio recalled

Medline Industries is recalling Medline Convenience Kits: Drawer 6 Central Line Insertio, distributed nationwide in the US. The recall was initiated on 6 May 2026 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codes1) ACC011142, UDI-DI: 10198459721342(each), 40198459721343(case), Lot Number: 26DDA462; 2) ACC011142, UDI-DI: 10198459721342(each), 40198459721343(case), Lot Number: 26DDA547; 3) DYNJ8407, UDI-DI: 10198459704543(each), 40198459704544(case), Lot Number: 26DBB599

Quantity recalled233 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-2454-2026
FDA event ID: 99043
Recalling firm: Medline Industries, Northfield, IL
Classification: Class I
Status: Ongoing
Recall initiated: 6 May 2026
FDA classified: 24 Jun 2026
Reported: 1 Jul 2026
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Processing Deviation
Device type: Other Medical Devices

Timeline

6 May 2026	Recall initiated by company
24 Jun 2026	Classified by FDA	+49 days
1 Jul 2026	Published in enforcement report	+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier.

The USDA issues these when meat or poultry was produced without proper inspection, or when a step such as cooking or pasteurisation did not meet requirements.

Product as listed by the FDA

Medline Convenience Kits: 1) DRAWER 6 CENTRAL LINE INSERTIO, Model Number: ACC011142; 2) CENTRAL AND ARTERIAL LINE TOTE, Model Number: DYNJ8407

Where it was distributed

US Nationwide.

Nationwide

Questions about this recall

Why was it recalled?

Which lots are affected?

1) ACC011142, UDI-DI: 10198459721342(each), 40198459721343(case), Lot Number: 26DDA462; 2) ACC011142, UDI-DI: 10198459721342(each), 40198459721343(case), Lot Number: 26DDA547; 3) DYNJ8407, UDI-DI: 10198459704543(each), 40198459704544(case), Lot Number: 26DBB599

Where was it sold?

US Nationwide.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

3 other products · FDA event 99043

This product is part of a recall event; the main page for the event is Medline Convenience Kits recalled by Medline Industries.

Reported	Class	Recall	Company	Reason	Where
1 Jul 2026	CLASS I	Medline Convenience Kits recalled by Medline Industries	Medline Industries	Processing Deviation	Nationwide
1 Jul 2026	CLASS I	Medline Convenience Kits: Drawer 6A Adult Central Line recalled	Medline Industries	Processing Deviation	Nationwide
1 Jul 2026	CLASS I	Medline Convenience Kits: Open Heart Cds recalled by Medline Industries	Medline Industries	Processing Deviation	Nationwide

More recalls from Medline Industries

All 709

Reported	Class	Recall	Company	Reason	Where
14 Oct 2026Device	CLASS II	Rollator, Bariatric, Basic Steel, Burgundy recalled	Medline Industries	Foreign Material	Nationwide
14 Oct 2026Device	CLASS II	Rollator, Bariatric, Basic Steel, Blue recalled by Medline Industries	Medline Industries	Foreign Material	Nationwide
7 Oct 2026Device	CLASS I	Medline Basic Homecare Beds and Medlite Homecare Beds recalled	Medline Industries	Device Malfunction	Nationwide
7 Oct 2026Device	CLASS I	Medline Basic Homecare Beds and Medlite Homecare Beds recalled	Medline Industries	Other	Nationwide
30 Sep 2026Device	CLASS II	Medline Convenience Kits: Major Pack recalled by Medline Industries	Medline Industries	Other	Nationwide

Other Other Medical Devices recalls

All 13,908

Reported	Class	Recall	Company	Reason	Where
14 Oct 2026Device	CLASS II	Plastics Tray kits recalled by Avid Medical	Avid Medical	Foreign Material	Nationwide
14 Oct 2026Device	CLASS II	Heart Prep Tray kits recalled by Avid Medical	Avid Medical	Other	Nationwide
14 Oct 2026Device	CLASS II	Pack Open Heart Cfh kits recalled by Avid Medical	Avid Medical	Other	Nationwide
14 Oct 2026Device	CLASS II	Sperm Ab Elisa (96 well plate test) recalled by DRG International	DRG International	Other	Nationwide
14 Oct 2026Device	CLASS III	BeneView Series recalled by Mindray DS USA	Mindray DS USA	Device Malfunction	Nationwide