FDAClass IIRecall started August 20, 2026

REF: 81-030415 Myocardial Probe Non-Pyrogenic Recall

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

Why was REF: 81-030415 Myocardial Probe Non-Pyrogenic recalled?

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

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

DI: 00749756046077/Lot # 63426754

Product
REF: 81-030415 Myocardial Probe Non-Pyrogenic , 400 Series
Recalling firm
DeRoyal Industries Inc
Quantity
7 cases, 140 units
Distribution
US Nationwide distribution in the states of LA,MO, MD, TN, UT.
Recall started
August 20, 2026
Report date
September 30, 2026
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls