Fresh Recalls

FDAClass II · Medical device · Recall Z-3256-2026 · Recalled September 30, 2026

REF recall — DeRoyal Industries Inc

Agency report date: September 30, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
REF
Company / brand
DeRoyal Industries
Lot / serial / date codes
DI: 00749756046077/Lot # 63426754
Distribution
US Nationwide distribution in the states of LA,MO, MD, TN, UT.
Agency product description and boundaries

REF: 81-030415 Myocardial Probe Non-Pyrogenic , 400 Series

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Myocardial temperature probes contain an incorrect needle. Specifically, an 18mm needle was included instead of a 15mm needle.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

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

Affected product: REF recall status

3. Open the official notice or contact

Official recall ID
Z-3256-2026
Brand
All DeRoyal Industries recalls
Classification
Class II
Units affected
7 cases, 140 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Powell, TN, United States
Firm address
200 Debusk Ln, 37849-4703

Identifying details (verbatim from the notice)

Product codes / lots
DI: 00749756046077/Lot # 63426754
Distribution
US Nationwide distribution in the states of LA,MO, MD, TN, UT.
Firm notified the public via
E-Mail
FDA event ID
99728
Recall initiated
August 20, 2026
FDA classified
September 22, 2026
FDA report date
September 30, 2026

Other medical device recalls from around the same time

Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 12:00 PM UTC. Record retrieved October 22, 2026 at 12:00 PM UTC.

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