Severity
Moderate
ModerateClass IIOngoing
FDA Devices recall · Reported May 14, 2025
Ambu aScope" 5 Broncho HD 5.6/2.8 Sampler Set. Model Number: 622002000US
Incorrect labeling in which the front red pouch label did not match the actual size of the medical device. The label on the front of the scope incorrectly states 5.0/2.2 while the…
Ambu Inc. recalled Ambu aScope" 5 Broncho HD 5.6/2.8 Sampler Set. Model Number: 622002000US - a moderate-severity action.
Ambu aScope" 5 Broncho HD 5.6/2.8 Sampler Set. Model Number: 622002000US was recalled by Ambu Inc. in May 14, 2025. Reason: Incorrect labeling in which the front red pouch label did not match the actual size of the medical device. Th…. Check the official notice for the remedy. Verify recall #Z-1723-2025 with the FDA Devices before acting.
The recall
Ambu Inc. issued this moderate-severity FDA Devices recall-Incorrect labeling in which the front red pouch label did not match the actual size of the medical device. Th….
- Moderate
- severity level
- 160 units
- affected scope
- Class II
- classification
- May 14, 2025
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1723-2025 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1723-2025) was formally reported on May 14, 2025, with the manufacturer initiating the action on April 7, 2025. 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 160 units.
The documented reason for this recall is: Incorrect labeling in which the front red pouch label did not match the actual size of the medical device. The label on the front of the scope incorrectly states 5.0/2.2 while the back label, shipping box and product in… Distribution data in the federal record shows the product reached: US Nationwide distribution in the states of CA, CO, FL, GA, KY, MD, MT, NJ, NV, PA, TN, TX, VA.. 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
160 units
Related Recalls
6
3 from same agency
Product description
Ambu aScope" 5 Broncho HD 5.6/2.8 Sampler Set. Model Number: 622002000US
Reason for recall
Incorrect labeling in which the front red pouch label did not match the actual size of the medical device. The label on the front of the scope incorrectly states 5.0/2.2 while the back label, shipping box and product inside correctly states 5.6/2.8.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-1723-2025 |
| Date reported | May 14, 2025 |
| Date initiated | April 7, 2025 |
| Recalling firm | Ambu Inc. |
| Firm location | Columbia, MD |
| Affected scope | 160 units |
| Distribution | US Nationwide distribution in the states of CA, CO, FL, GA, KY, MD, MT, NJ, NV, PA, TN, TX, VA. |
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-1723-2025) 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 aScope" 5 Broncho HD 5.6/2.8 Sampler Set. Model Number: 622002000US. Recalled by Ambu Inc.. Units affected: 160 units.
Why was this product recalled? ▼
Incorrect labeling in which the front red pouch label did not match the actual size of the medical device. The label on the front of the scope incorrectly states 5.0/2.2 while the back label, shipping box and product inside correctly states 5.6/2.8.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 14, 2025. Severity: Moderate. Recall number: Z-1723-2025.
Where was the recalled product distributed? ▼
Distribution: US Nationwide distribution in the states of CA, CO, FL, GA, KY, MD, MT, NJ, NV, PA, TN, TX, VA..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1723-2025) 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 May 14, 2025. 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.