FreshRecalls

⚠ Data freshness notice: the most recent refresh of NHTSA was incomplete, so a very recent recall may be missing. Everything shown is accurate as of the last checked time on this page — for anything time-critical, confirm with the official sources linked below.

FDAClass II · Medical device · Recalled July 15, 2026

Medline Convenience Kits recall — Medline Industries, LP

Hazard: Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm general purpose temperature probe-size 9 due to an error in its distribution control process.

Class II: may cause temporary or medically reversible health consequences.

Official recall ID
Z-2696-2026
Brand
Medline Industries
Classification
Class II
Units affected
75 kits
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Description

Medline Convenience Kits: 1) OPEN HEART PEDS PACK, Model Number: DYNJ88569D; 2) ACCESSORY KIT, Model Number: DYNJ901348F

Affected products

Companies & origin

Recalling firm location
Northfield, IL, United States
Firm address
3 Lakes Dr, N/A, 60093-2753

Identifying details (verbatim from the notice)

Product codes / lots
1) DYNJ88569D, UDI-DI: 10198459745775(each), 40198459745776(case), Lot Number: 26DBP363; 2) DYNJ901348F, UDI-DI: 10198459216213(each), 40198459216214(case), Lot Number: 25JBQ159
Distribution
US Nationwide distribution.
Firm notified the public via
N/A
FDA event ID
99196
Recall initiated
May 28, 2026
FDA classified
July 8, 2026
FDA report date
July 15, 2026

Source: U.S. Food & Drug Administration. This page mirrors the official public-domain record verbatim; the linked government source is authoritative. Source last checked July 23, 2026 at 11:04 PM UTC.

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