Severity
Moderate
ModerateClass IIOngoing
FDA Devices recall · Reported April 24, 2024
RENASYS EDGE 800ML CANISTER WITH Solidifier- Indicated for patients who would benefit from a suction pump (NPWT), as it may promote wound healing Product Number: 66803140
Black particulate matter from the carbon filter component of the canisters entering the NPWT pump and potentially causing damage to the pump
Smith & Nephew Medical, Ltd. recalled RENASYS EDGE 800ML CANISTER WITH Solidifier- Indicated for patients who would benefit fro… - a moderate-severity action.
RENASYS EDGE 800ML CANISTER WITH Solidifier- Indicated for patients who would benefit fro… was recalled by Smith & Nephew Medical, Ltd. in April 24, 2024. Reason: Black particulate matter from the carbon filter component of the canisters entering the NPWT pump and potenti…. Check the official notice for the remedy. Verify recall #Z-1597-2024 with the FDA Devices before acting.
The recall
Smith & Nephew Medical, Ltd. issued this moderate-severity FDA Devices recall-Black particulate matter from the carbon filter component of the canisters entering the NPWT pump and potenti….
- Moderate
- severity level
- 675 units
- affected scope
- Class II
- classification
- April 24, 2024
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1597-2024 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1597-2024) was formally reported on April 24, 2024, with the manufacturer initiating the action on March 11, 2024. It is classified under Moderate severity (Class II), with a current status of Ongoing. Smith & Nephew Medical, Ltd. is listed as the recalling firm, operating out of Hull. Federal records list the affected scope as 675 units.
The documented reason for this recall is: Black particulate matter from the carbon filter component of the canisters entering the NPWT pump and potentially causing damage to the pump Distribution data in the federal record shows the product reached: Worldwide distribution - US Nationwide and the countries of Canada, Chile.. 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
675 units
Related Recalls
6
3 from same agency
Product description
RENASYS EDGE 800ML CANISTER WITH Solidifier- Indicated for patients who would benefit from a suction pump (NPWT), as it may promote wound healing Product Number: 66803140
Reason for recall
Black particulate matter from the carbon filter component of the canisters entering the NPWT pump and potentially causing damage to the pump
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-1597-2024 |
| Date reported | April 24, 2024 |
| Date initiated | March 11, 2024 |
| Recalling firm | Smith & Nephew Medical, Ltd. |
| Firm location | Hull |
| Affected scope | 675 units |
| Distribution | Worldwide distribution - US Nationwide and the countries of Canada, Chile. |
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-1597-2024) 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? ▼
RENASYS EDGE 800ML CANISTER WITH Solidifier- Indicated for patients who would benefit from a suction pump (NPWT), as it may promote wound healing Product Number: 66803140. Recalled by Smith & Nephew Medical, Ltd.. Units affected: 675 units.
Why was this product recalled? ▼
Black particulate matter from the carbon filter component of the canisters entering the NPWT pump and potentially causing damage to the pump
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 24, 2024. Severity: Moderate. Recall number: Z-1597-2024.
Where was the recalled product distributed? ▼
Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Chile..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1597-2024) 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 April 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.