Severity
Moderate
ModerateClass IIOngoing
FDA Devices recall · Reported January 17, 2024
Ambu aView 2 A Monitor, Catalog numbers 405011000 and 405011000US2
Instructions for Use have been updated to add the following warning: Use only M4 screws with the length of 14 16 mm when mounting Ambu aView 2 Advance on a VESA interface. Using…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Ambu Inc. recalled Ambu aView 2 A Monitor, Catalog numbers 405011000 and 405011000US2 - a moderate-severity action.
Ambu aView 2 A Monitor, Catalog numbers 405011000 and 405011000US2 was recalled by Ambu Inc. in January 17, 2024. Reason: Instructions for Use have been updated to add the following warning: Use only M4 screws with the length of 14…. Check the official notice for the remedy. Verify recall #Z-0714-2024 with the FDA Devices before acting.
The recall
Ambu Inc. issued this moderate-severity FDA Devices recall-Instructions for Use have been updated to add the following warning: Use only M4 screws with the length of 14….
- Moderate
- severity level
- Class II
- classification
- January 17, 2024
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0714-2024 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0714-2024) was formally reported on January 17, 2024, with the manufacturer initiating the action on December 5, 2023. It is classified under Moderate severity (Class II), with a current status of Ongoing. Ambu Inc. is listed as the recalling firm, operating out of Columbia, MD. Federal records list the affected scope as 11845 distributed US.
The documented reason for this recall is: Instructions for Use have been updated to add the following warning: Use only M4 screws with the length of 14 16 mm when mounting Ambu aView 2 Advance on a VESA interface. Using longer screw lengths will penetrate the… Distribution data in the federal record shows the product reached: Domestic distribution nationwide.. 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
11845 distributed US
Related Recalls
6
3 from same agency
Product description
Ambu aView 2 A Monitor, Catalog numbers 405011000 and 405011000US2
Reason for recall
Instructions for Use have been updated to add the following warning: Use only M4 screws with the length of 14 16 mm when mounting Ambu aView 2 Advance on a VESA interface. Using longer screw lengths will penetrate the lithium-ion battery and result in a fire hazard and battery leakage which can cause severe burns, smoke inhalation and skin irritation. Using shorter screw lengths could result in unsecure device fastening.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-0714-2024 |
| Date reported | January 17, 2024 |
| Date initiated | December 5, 2023 |
| Recalling firm | Ambu Inc. |
| Firm location | Columbia, MD |
| Affected scope | 11845 distributed US |
| Distribution | Domestic distribution nationwide. |
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-0714-2024) 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? ▼
Ambu aView 2 A Monitor, Catalog numbers 405011000 and 405011000US2. Recalled by Ambu Inc.. Units affected: 11845 distributed US.
Why was this product recalled? ▼
Instructions for Use have been updated to add the following warning: Use only M4 screws with the length of 14 16 mm when mounting Ambu aView 2 Advance on a VESA interface. Using longer screw lengths will penetrate the lithium-ion battery and result in a fire hazard and battery leakage which can cause severe burns, smoke inhalation and skin irritation. Using shorter screw lengths could result in unsecure device fastening.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on January 17, 2024. Severity: Moderate. Recall number: Z-0714-2024.
Where was the recalled product distributed? ▼
Distribution: Domestic distribution nationwide..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0714-2024) 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 17, 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.