Recall events
/
Event 76476
Event summary
Timeline bucket February 07, 2017
Product types Device
Classifications Class II
Statuses Terminated
Recalling firm wording LeMaitre Vascular, Inc.
Dossier provenance
Source snapshots represented here
openFDA Device Enforcement
Report-date coverage
June 20, 2012–July 08, 2026
Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
openFDA Device Recall
event_date_initiated coverage
June 01, 1997–June 30, 2026
Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.
How coverage and grouping work
Complete imported group
Every recalled product in this event
12 official enforcement rows
Product dates, classifications, firms, and source wording remain attached to their individual rows.
Opening this dossier never hides products that did not match a prior timeline filter.
device · product 1 of 12
LeMaitre Vascular Reddick Cholangiogram Catheter (eIFU) REF# e2400-50
Z-1442-2017
Recall number Z-1442-2017
Initiated February 07, 2017
Classification Class II
Status Terminated
Quantity 5601
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Labeling design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1442-2017
Source locator 0001-device-recall-0001-of-0001.json.zip#results[44380]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
Code information Lot Number/Exp. Date: RED1743 2018-09 RED1744 2018-09 RED1749 2018-10 RED1750 2018-12 RED1751 2018-12 RED1755 2018-12 RED1756 2018-12 RED1757 2019-01 RED1759 2019-02 RED1760 2019-02 RED1761 2019-03 RED1764 2019-03 RED1766 2019-04 RED1767 2019-04 RED1768 2019-05 RED1769 2019-05 RED1771 2019-06 RED1773 2019-07 RED1774 2019-07 RED1775 2019-07
Distribution pattern Worldwide distribution. US Nationwide, AUSTRIA, BELGIUM, FRANCE, GERMANY, ITALY, LUXEMBOURG, Morocco, Saudi Arabia, Singapore, SPAIN, SWITZERLAND, UAE, and UK
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[19041]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 12
LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter (eIFU) REF# e2400-51
Z-1443-2017
Recall number Z-1443-2017
Initiated February 07, 2017
Classification Class II
Status Terminated
Quantity 340
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Labeling design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1443-2017
Source locator 0001-device-recall-0001-of-0001.json.zip#results[4101]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
Code information Lot Number/Exp. Date: RED1752 2018-12 RED1758 2019-01 RED1772 2019-06
Distribution pattern Worldwide distribution. US Nationwide, AUSTRIA, BELGIUM, FRANCE, GERMANY, ITALY, LUXEMBOURG, Morocco, Saudi Arabia, Singapore, SPAIN, SWITZERLAND, UAE, and UK
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20272]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 12
LeMaitre Vascular Reddick Cholangiogram Catheter with introducer(eIFU) REF # e2400-52
Z-1444-2017
Recall number Z-1444-2017
Initiated February 07, 2017
Classification Class II
Status Terminated
Quantity 608
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Labeling design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1444-2017
Source locator 0001-device-recall-0001-of-0001.json.zip#results[34096]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
Code information Lot Number/Ex Date: RED1746 2018-09 RED1753 2018-12 RED1762 2019-03 RED1765 2019-03 RED1779 2019-09
Distribution pattern Worldwide distribution. US Nationwide, AUSTRIA, BELGIUM, FRANCE, GERMANY, ITALY, LUXEMBOURG, Morocco, Saudi Arabia, Singapore, SPAIN, SWITZERLAND, UAE, and UK
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[19884]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 12
LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer (eIFU) REF # e2400-53
Z-1445-2017
Recall number Z-1445-2017
Initiated February 07, 2017
Classification Class II
Status Terminated
Quantity 250
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Labeling design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1445-2017
Source locator 0001-device-recall-0001-of-0001.json.zip#results[34093]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
Code information Lot Number/Ex p. Date: RED1747 2018-09 RED1754 2018-12 RED1763 2019-03 RED1770 2019-05
Distribution pattern Worldwide distribution. US Nationwide, AUSTRIA, BELGIUM, FRANCE, GERMANY, ITALY, LUXEMBOURG, Morocco, Saudi Arabia, Singapore, SPAIN, SWITZERLAND, UAE, and UK
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[25740]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 12
LeMaitre Vascular Reddick Scoop Tip Cholangiogram Catheter (eIFU) REF# e2401-50
Z-1446-2017
Recall number Z-1446-2017
Initiated February 07, 2017
Classification Class II
Status Terminated
Quantity 4673
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Labeling design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1446-2017
Source locator 0001-device-recall-0001-of-0001.json.zip#results[10361]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
Code information Lot Number/Ex p. Date: RST2390 2018-08 RST2393 2018-09 RST2396 2018-10 RST2397 2018-10 RST2398 2018-10 RST2401 2018-12 RST2402 2018-12 RST2418 2019-02 RST2420 2019-03 RST2423 2019-03 RST2428 2019-04 RST2432 2019-04 RST2433 2019-04 RST2437 2019-06 RST2438 2019-06 RST2441 2019-07
Distribution pattern Worldwide distribution. US Nationwide, AUSTRIA, BELGIUM, FRANCE, GERMANY, ITALY, LUXEMBOURG, Morocco, Saudi Arabia, Singapore, SPAIN, SWITZERLAND, UAE, and UK
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[24359]
FDA event record
· Exact recall-number query on openFDA
device · product 6 of 12
LeMaitre Vascular Reddick Scoop Tip Cholangiogram Stiffer Catheter (paper IFU) REF# 2401-50
Z-1447-2017
Recall number Z-1447-2017
Initiated February 07, 2017
Classification Class II
Status Terminated
Quantity 403
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Labeling design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1447-2017
Source locator 0001-device-recall-0001-of-0001.json.zip#results[10363]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
Code information Lot Number/Exp. Date: RST2404 2018-012 RST2416 2019-02 RST2424 2019-03 RST2426 2019-03 RST2442 2019-07
Distribution pattern Worldwide distribution. US Nationwide, AUSTRIA, BELGIUM, FRANCE, GERMANY, ITALY, LUXEMBOURG, Morocco, Saudi Arabia, Singapore, SPAIN, SWITZERLAND, UAE, and UK
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[24369]
FDA event record
· Exact recall-number query on openFDA
device · product 7 of 12
LeMaitre Vascular Reddick Scoop Tip Cholangiogram Catheter with Introducer (eIFU) REF# e2401-51
Z-1448-2017
Recall number Z-1448-2017
Initiated February 07, 2017
Classification Class II
Status Terminated
Quantity 2065
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Labeling design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1448-2017
Source locator 0001-device-recall-0001-of-0001.json.zip#results[34092]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
Code information Lot Number/Exp. Date: RST2403 2018-12 RST2409 2019-01 RST2410 2019-01 RST2427 2019-03 RST2434 2019-05 RST2439 2019-06 RST2444 2019-07
Distribution pattern Worldwide distribution. US Nationwide, AUSTRIA, BELGIUM, FRANCE, GERMANY, ITALY, LUXEMBOURG, Morocco, Saudi Arabia, Singapore, SPAIN, SWITZERLAND, UAE, and UK
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[24364]
FDA event record
· Exact recall-number query on openFDA
device · product 8 of 12
LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer (paper IFU) REF# 2401-51
Z-1449-2017
Recall number Z-1449-2017
Initiated February 07, 2017
Classification Class II
Status Terminated
Quantity 179
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Labeling design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1449-2017
Source locator 0001-device-recall-0001-of-0001.json.zip#results[34094]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
Code information Lot Number/Exp. Date: RST2405 2018-12 RST2417 2019-02 RST2425 2019-03 RST2449 2019-08
Distribution pattern Worldwide distribution. US Nationwide, AUSTRIA, BELGIUM, FRANCE, GERMANY, ITALY, LUXEMBOURG, Morocco, Saudi Arabia, Singapore, SPAIN, SWITZERLAND, UAE, and UK
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[24154]
FDA event record
· Exact recall-number query on openFDA
device · product 9 of 12
LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (eIFU) REF# e2401-52
Z-1450-2017
Recall number Z-1450-2017
Initiated February 07, 2017
Classification Class II
Status Terminated
Quantity 4673
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Labeling design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1450-2017
Source locator 0001-device-recall-0001-of-0001.json.zip#results[44377]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
Code information Lot Number/Exp. Date: RST2391 2018-09 RST2394 2018-09 RST2395 2018-09 RST2406 2018-12 RST2407 2018-12 RST2414 2019-02 RST2415 2019-02 RST2421 2019-03 RST2422 2019-03 RST2429 2019-04 RST2430 2019-04 RST2435 2019-05 RST2445 2019-07 RST2446 2019-07 RST2451 2019-08
Distribution pattern Worldwide distribution. US Nationwide, AUSTRIA, BELGIUM, FRANCE, GERMANY, ITALY, LUXEMBOURG, Morocco, Saudi Arabia, Singapore, SPAIN, SWITZERLAND, UAE, and UK
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[25746]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1451-2017
Initiated February 07, 2017
Classification Class II
Status Terminated
Quantity 247
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Labeling design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1451-2017
Source locator 0001-device-recall-0001-of-0001.json.zip#results[4102]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
Code information Lot Number/Exp. Date: RST2394 2018-09 RST2411 2019-01 RST2412 2019-01 RST2459 2019-10
Distribution pattern Worldwide distribution. US Nationwide, AUSTRIA, BELGIUM, FRANCE, GERMANY, ITALY, LUXEMBOURG, Morocco, Saudi Arabia, Singapore, SPAIN, SWITZERLAND, UAE, and UK
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[24222]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1452-2017
Initiated February 07, 2017
Classification Class II
Status Terminated
Quantity 2065
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Labeling design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1452-2017
Source locator 0001-device-recall-0001-of-0001.json.zip#results[4100]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
Code information Lot Number/Exp. Date: RST2392 2018-09 RST2400 2018-10 RST2408 2018-12 RST2419 2019-04 RST2431 2019-04 RST2436 2019-05 RST2447 2019-08
Distribution pattern Worldwide distribution. US Nationwide, AUSTRIA, BELGIUM, FRANCE, GERMANY, ITALY, LUXEMBOURG, Morocco, Saudi Arabia, Singapore, SPAIN, SWITZERLAND, UAE, and UK
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[19893]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-1453-2017
Initiated February 07, 2017
Classification Class II
Status Terminated
Quantity 46
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Labeling design
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1453-2017
Source locator 0001-device-recall-0001-of-0001.json.zip#results[34091]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
Code information Lot Number/Exp. Date: RST2413 2019-01
Distribution pattern Worldwide distribution. US Nationwide, AUSTRIA, BELGIUM, FRANCE, GERMANY, ITALY, LUXEMBOURG, Morocco, Saudi Arabia, Singapore, SPAIN, SWITZERLAND, UAE, and UK
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[26197]
FDA event record
· Exact recall-number query on openFDA
