Severity
Moderate
ModerateClass IIOngoing
FDA Devices recall · Reported January 24, 2024
HIGH PRESSURE ROTATOR WITH FEMALE LUER LOCK, List Number MX497HP
There is a manufacturing defect affecting specific rotator lots. Within this population, the inner diameter of the devices O-ring may be oversized affecting seal integrity. An in…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Smiths Medical Asd Inc recalled HIGH PRESSURE ROTATOR WITH FEMALE LUER LOCK, List Number MX497HP - a moderate-severity action.
HIGH PRESSURE ROTATOR WITH FEMALE LUER LOCK, List Number MX497HP was recalled by Smiths Medical Asd Inc in January 24, 2024. Reason: There is a manufacturing defect affecting specific rotator lots. Within this population, the inner diameter o…. Check the official notice for the remedy. Verify recall #Z-0744-2024 with the FDA Devices before acting.
The recall
Smiths Medical Asd Inc issued this moderate-severity FDA Devices recall-There is a manufacturing defect affecting specific rotator lots. Within this population, the inner diameter o….
- Moderate
- severity level
- Class II
- classification
- January 24, 2024
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0744-2024 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0744-2024) was formally reported on January 24, 2024, with the manufacturer initiating the action on November 10, 2023. It is classified under Moderate severity (Class II), with a current status of Ongoing. Smiths Medical Asd Inc is listed as the recalling firm, operating out of Dublin, OH. Federal records list the affected scope as 31,685 total.
The documented reason for this recall is: There is a manufacturing defect affecting specific rotator lots. Within this population, the inner diameter of the devices O-ring may be oversized affecting seal integrity. An inadequate seal may lead to a leak during … Distribution data in the federal record shows the product reached: Worldwide distribution - US Nationwide and the countries of Canada, UAE.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
31,685 total
Related Recalls
6
3 from same agency
Product description
HIGH PRESSURE ROTATOR WITH FEMALE LUER LOCK, List Number MX497HP
Reason for recall
There is a manufacturing defect affecting specific rotator lots. Within this population, the inner diameter of the devices O-ring may be oversized affecting seal integrity. An inadequate seal may lead to a leak during infusion of medication which may potentially lead to under infusion of medication.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-0744-2024 |
| Date reported | January 24, 2024 |
| Date initiated | November 10, 2023 |
| Recalling firm | Smiths Medical Asd Inc |
| Firm location | Dublin, OH |
| Affected scope | 31,685 total |
| Distribution | Worldwide distribution - US Nationwide and the countries of Canada, UAE. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-0744-2024) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
HIGH PRESSURE ROTATOR WITH FEMALE LUER LOCK, List Number MX497HP. Recalled by Smiths Medical Asd Inc. Units affected: 31,685 total.
Why was this product recalled? ▼
There is a manufacturing defect affecting specific rotator lots. Within this population, the inner diameter of the devices O-ring may be oversized affecting seal integrity. An inadequate seal may lead to a leak during infusion of medication which may potentially lead to under infusion of medication.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on January 24, 2024. Severity: Moderate. Recall number: Z-0744-2024.
Where was the recalled product distributed? ▼
Distribution: Worldwide distribution - US Nationwide and the countries of Canada, UAE..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0744-2024) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported January 24, 2024. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.