DeRoyal Industries recall: REF: 81-030415 Myocardial Probe Non-Pyrogenic
DeRoyal Industries Inc is recalling REF: 81-030415 Myocardial Probe Non-Pyrogenic – 7 cases, 140 units. The U.S. Food and Drug Administration published the recall on September 30, 2026; it began on August 20, 2026. Distributed nationwide.
Serious Class II means the product may cause temporary or medically reversible health problems, or the chance of serious harm is remote.
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| Product | REF: 81-030415 Myocardial Probe Non-Pyrogenic |
| Brand | DeRoyal Industries |
| Company | DeRoyal Industries Inc |
| Type | Medical devices |
| Classification | Class II |
| Recall date | August 20, 2026 |
| Published by FDA | September 30, 2026 |
| Quantity | 7 cases, 140 units |
| Recall ID | 99728 |
Recalled products
- REF: 81-030415 Myocardial Probe Non-Pyrogenic , 400 Series
- FDA recall number
- Z-3256-2026
- Codes, lots and dates
- DI: 00749756046077/Lot # 63426754
- Quantity
- 7 cases, 140 units
- Classification
- Class II
Identifiers and details
- FDA event ID
- 99728
- Initiated
- Voluntary: Firm initiated
- Status
- Ongoing
- Firm location
- Powell, TN, United States
Why it was recalled
The reason the FDA lists: “Myocardial temperature probes contain an incorrect needle. Specifically, an 18mm needle was included instead of a 15mm needle.”
Where it was sold
Nationwide. Distribution as the FDA records it: “US Nationwide distribution in the states of LA,MO, MD, TN, UT.”
What to do
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Official notice: FDA Enforcement Report record (event 99728, openFDA) – the same recall numbers can be searched in the FDA Enforcement Report.
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|---|---|---|---|
| Oct 7, 2026 |  Draeger recall: VentStar Resus NeoMedical devices · 1,063,643 units | Potential cracks in the hose, which could lead to leakage or the hose falling off. Most serious | FDA Class I |
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| Oct 7, 2026 | Karl Storz Endoscopy recall: HOPKINS Telescope 30¿Medical devices · 6 eyepieces | Due to incorrect inside packaging label for eyepiece. Serious | FDA Class II |
| Oct 7, 2026 | Noxbox recall: NOxBOXi Nitric Oxide Delivery SystemMedical devices · 1,667 units | Potential for irregular oxygen readings due to a manufacturing issue affecting certain oxy… Serious | FDA Class II |
| Oct 7, 2026 | Siemens Healthcare Diagnostics recall: Atellica CH Revised C-Reactive ProteinMedical devices · 42940 units (3938 US, 39002 OUS) | The potential for falsely elevated results. Serious | FDA Class II |
| Oct 7, 2026 | Tandem Diabetes Care recall: T:slim Mobile ApplicationMedical devices · 177 | A beta (early-release) version of the iOS application, version 2.13 (TestFlight) had a sof… Serious | FDA Class II |
About this recall
Is DeRoyal Industries REF: 81-030415 Myocardial Probe Non-Pyrogenic recalled?
Yes. DeRoyal Industries Inc recalled it on August 20, 2026; FDA published it September 30, 2026 (Class II). Only the lots, dates or models listed on this page are included.
Why was it 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 it?
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Where was it sold?
Nationwide.
More recalls
Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.