CLASS II ONGOING Device recall · Reported 3 Aug 2022 · FDA Enforcement Report

Medline convenience kits recalled by Medline Industries, Lp - Spt

Medline Industries, Lp - Spt is recalling Medline convenience kits: a, distributed nationwide in the US. The recall was initiated on 6 Jun 2022 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Code: a. Model Number DYNJ36725B, Lot codes: 19UBB149, b. Model Number DYNJ905860A, Lot codes: 22OBG246, 21LBU048, 21GBI196, 21KBK242, 21EBH567

Quantity recalled288 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-1471-2022
FDA event ID: 90516
Recalling firm: Medline Industries, Lp - Spt, Waukegan, IL
Classification: Class II
Status: Ongoing
Recall initiated: 6 Jun 2022
FDA classified: 27 Jul 2022
Reported: 3 Aug 2022
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Packaging Defects
Device type: Other Medical Devices

Timeline

6 Jun 2022	Recall initiated by company
27 Jul 2022	Classified by FDA	+51 days
3 Aug 2022	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

Kits contain leaking bottles of isopropyl alcohol

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

Medline convenience kits: a. VENOUS ACCESS PACK-LF, Model Number DYNJ36725B, Lot codes: 19UBB149, b. KIT LB SHUNT, Model NumberDYNJ905860A, Lot codes: 22OBG246, 21LBU048, 21GBI196, 21KBK242, 21EBH567 Model/Catalog Number: a. Model Number DYNJ36725B, b. Model Number DYNJ905860A

Where it was distributed

US Nationwide distribution.

Nationwide

Questions about this recall

Is Medline convenience kits: a recalled?

Yes. Medline Industries, Lp - Spt recalled Medline convenience kits: a on 6 Jun 2022. The recall is Class II and its status is Ongoing. Recall number Z-1471-2022.

Why was it recalled?

Kits contain leaking bottles of isopropyl alcohol

Which lots are affected?

Lot Code: a. Model Number DYNJ36725B, Lot codes: 19UBB149, b. Model Number DYNJ905860A, Lot codes: 22OBG246, 21LBU048, 21GBI196, 21KBK242, 21EBH567

Where was it sold?

US Nationwide distribution.

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

More recalls from Medline Industries, Lp - Spt

All 8

Reported	Class	Recall	Company	Reason	Where
3 Aug 2022Device	CLASS II	Medline convenience kits labeled as recalled	Medline Industries, Lp - Spt	Packaging Defects	Nationwide
3 Aug 2022Device	CLASS II	Medline convenience kits labeled as: LAP Chole recalled	Medline Industries, Lp - Spt	Packaging Defects	Nationwide
3 Aug 2022Device	CLASS II	Medline Convenience kits labeled as recalled	Medline Industries, Lp - Spt	Packaging Defects	Nationwide
3 Aug 2022Device	CLASS II	Recalled product recalled by Medline Industries, Lp - Spt	Medline Industries, Lp - Spt	Packaging Defects	Nationwide
3 Aug 2022Device	CLASS II	Medline Custom procedural kits labeled as follows recalled	Medline Industries, Lp - Spt	Packaging Defects	Nationwide

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