Severity
Moderate
ModerateClass IIOngoing
FDA Devices recall · Reported May 21, 2025
Pruitt Irrigation Occlusion Catheter. Catalog Numbers: 2102-09, E2102-09.
During internal product testing, it was observed that some packages to have incomplete seals (sterile barrier).
LeMaitre Vascular, Inc. recalled Pruitt Irrigation Occlusion Catheter. Catalog Numbers: 2102-09, E2102-09. - a moderate-severity action.
Pruitt Irrigation Occlusion Catheter. Catalog Numbers: 2102-09, E2102-09. was recalled by LeMaitre Vascular, Inc. in May 21, 2025. Reason: During internal product testing, it was observed that some packages to have incomplete seals (sterile barrier…. Check the official notice for the remedy. Verify recall #Z-1752-2025 with the FDA Devices before acting.
The recall
LeMaitre Vascular, Inc. issued this moderate-severity FDA Devices recall-During internal product testing, it was observed that some packages to have incomplete seals (sterile barrier….
- Moderate
- severity level
- 27K units
- affected scope
- Class II
- classification
- May 21, 2025
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1752-2025 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1752-2025) was formally reported on May 21, 2025, with the manufacturer initiating the action on April 11, 2025. It is classified under Moderate severity (Class II), with a current status of Ongoing. LeMaitre Vascular, Inc. is listed as the recalling firm, operating out of Burlington, MA. Federal records list the affected scope as 26,872 units.
The documented reason for this recall is: During internal product testing, it was observed that some packages to have incomplete seals (sterile barrier). Distribution data in the federal record shows the product reached: Nationwide distribution. International distribution to ARGENTINA, AUSTRALIA, AUSTRIA, BELGIUM, BRAZIL, BULGARIA, CAMBODIA, CANADA, CHILE, COLOMBIA, COSTA RICA, CYPRUS, CZECHIA, DENMARK, DOMINICAN REPUBLIC, EGYPT, EL SAL…. 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
26,872 units
Related Recalls
6
3 from same agency
Product description
Pruitt Irrigation Occlusion Catheter. Catalog Numbers: 2102-09, E2102-09.
Reason for recall
During internal product testing, it was observed that some packages to have incomplete seals (sterile barrier).
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-1752-2025 |
| Date reported | May 21, 2025 |
| Date initiated | April 11, 2025 |
| Recalling firm | LeMaitre Vascular, Inc. |
| Firm location | Burlington, MA |
| Affected scope | 26,872 units |
| Distribution | Nationwide distribution. International distribution to ARGENTINA, AUSTRALIA, AUSTRIA, BELGIUM, BRAZIL, BULGARIA, CAMBODIA, CANADA, CHILE, COLOMBIA, COSTA RICA, CYPRUS, CZECHIA, DENMARK, DOMINICAN REPUBLIC, EGYPT, EL SALVADOR, ESTONIA, FINL… |
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-1752-2025) 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? ▼
Pruitt Irrigation Occlusion Catheter. Catalog Numbers: 2102-09, E2102-09.. Recalled by LeMaitre Vascular, Inc.. Units affected: 26,872 units.
Why was this product recalled? ▼
During internal product testing, it was observed that some packages to have incomplete seals (sterile barrier).
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 21, 2025. Severity: Moderate. Recall number: Z-1752-2025.
Where was the recalled product distributed? ▼
Distribution: Nationwide distribution. International distribution to ARGENTINA, AUSTRALIA, AUSTRIA, BELGIUM, BRAZIL, BULGARIA, CAMBODIA, CANADA, CHILE, COLOMBIA, COSTA RICA, CYPRUS, CZECHIA, DENMARK, DOMINICAN REPUBLIC, EGYPT, EL SALVADOR, ESTONIA, FINLAND, FRANCE, GEORGIA, GERMANY, GREECE, GUATEMALA, GUYANA, HONG KONG, HUNGARY, INDIA, INDONESIA, IRELAND, ISRAEL, ITALY, JAPAN, JORDAN, KUWAIT, LATVIA, LEBANON, LITHUANIA, MALAYSIA, MALTA, MEXICO, MONGOLIA, MOROCCO, NETHERLANDS, NEW ZEALAND, NICARAGUA, NORTH MACEDONIA, NORWAY, OMAN, PANAMA, PARAGUAY, PHILIPPINES, POLAND, QATAR, ROMANIA, RUSSIA, SAUDI ARABIA, SERBIA, SINGAPORE, SLOVAKIA, SLOVENIA, SOUTH AFRICA, SOUTH KOREA, SPAIN, SWEDEN, SWITZERLAND, TAIWAN, THAILAND, TRINIDAD AND TOBAGO, TUNISIA, TURKIYE, UNITED ARAB EMIRATES, UNITED KINGDOM, VENEZUELA, VIETNAM..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1752-2025) 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 21, 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.