DeRoyal Myocardial Probe Recall Due to Incorrect Needle Length
DeRoyal Industries is recalling Myocardial Probes that contain an 18mm needle instead of the specified 15mm needle.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, and the source text does not report any illnesses or injuries, fitting the criteria for a moderate severity score.
Plain-English summary
DeRoyal Industries Inc is recalling 7 cases, or 140 units, of Myocardial Probe Non-Pyrogenic, 400 Series (REF: 81-030415). The recall is due to a manufacturing error where the probes were packaged with an 18mm needle instead of the required 15mm needle.
The affected units are identified by DI 00749756046077 and Lot # 63426754. These products were distributed nationwide in the states of Louisiana, Missouri, Maryland, Tennessee, and Utah.
Healthcare facilities and consumers should stop using the affected probes and contact DeRoyal Industries for further instructions or a return.
The recalled product
- Product
- REF: 81-030415 Myocardial Probe Non-Pyrogenic , 400 Series
- Manufacturer
- DeRoyal Industries Inc
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- DI: 00749756046077/Lot # 63426754
Distribution
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