Recall events
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Event 98631
Event summary
Timeline bucket March 09, 2026
Product types Device
Classifications Class II
Statuses Ongoing
Recalling firm wording LSL Healthcare 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
6 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 6
LSL Healthcare, Central Line Dressing Kit, Model/Catalog Number: 2717H
Z-1928-2026
Recall number Z-1928-2026
Initiated March 09, 2026
Classification Class II
Status Ongoing
Quantity 3880 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1928-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[23476]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
Code information Lot Code: Model No. 2717H; UDI-DI 00661392054738; Lot# 6A3181; Expiration Date 11/30/2026 GTIN: (01)00661392054738(10)6A3181(17)261130
Distribution pattern US Nationwide distribution in the states of MD, IL, MN.
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[726]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 6
LSL Healthcare, Standard Central Line Dressing Change Kit, Model/Catalog Number: 2717J
Z-1929-2026
Recall number Z-1929-2026
Initiated March 09, 2026
Classification Class II
Status Ongoing
Quantity 3460 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1929-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[29337]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
Code information Lot Code: Model No. 2717J; UDI-DI 00661392054721; Lot# 6A3043, Expiration Date 11/30/2026. Lot#6B3076, Expiration Date 01/31/2027 GTIN: (01)00661392054721(10)6A3043(17)261130 GTIN: (01)00661392054721(10)6B3076(17)260131
Distribution pattern US Nationwide distribution in the states of MD, IL, MN.
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[742]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 6
LSL Healthcare, Foley Urine Collection Kit, Model/Catalog Number: 1555
Z-1930-2026
Recall number Z-1930-2026
Initiated March 09, 2026
Classification Class II
Status Ongoing
Quantity 100 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1930-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5906]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
Code information Lot Code: Model No. 1555; UDI-DI 00661392002326; Lot# 260221, Expiration Date 02/28/2027 GTIN: (01)00661392002326(10)260221(17)270228
Distribution pattern US Nationwide distribution in the states of MD, IL, MN.
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[669]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 6
LSL Healthcare, Infant Central Line Dressing Change Kit, Model/Catalog Number: 2925H
Z-1931-2026
Recall number Z-1931-2026
Initiated March 09, 2026
Classification Class II
Status Ongoing
Quantity 220 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1931-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[29335]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
Code information Lot Code: Model No. 2925H; UDI-DI 00661392052635; Lot#6B3022, Expiration Date 11/30/2026 GTIN: (01)00661392052635(10)6B3022(17)261130
Distribution pattern US Nationwide distribution in the states of MD, IL, MN.
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[744]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 6
LSL Healthcare, IV Start Kit, Model/Catalog Number: 3131
Z-1932-2026
Recall number Z-1932-2026
Initiated March 09, 2026
Classification Class II
Status Ongoing
Quantity 2200 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1932-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[56198]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
Code information Lot Code: Model No. 3131; UDI-DI 00661392054271; Lot#6A3139, Expiration Date 01/21/2028 GTIN: (01)00661392054271(10)6A3139(17)280121
Distribution pattern US Nationwide distribution in the states of MD, IL, MN.
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[733]
FDA event record
· Exact recall-number query on openFDA
device · product 6 of 6
LSL Healthcare Wound Closure Tray, Model/Catalog Number: 7554
Z-1933-2026
Recall number Z-1933-2026
Initiated March 09, 2026
Classification Class II
Status Ongoing
Quantity 200 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1933-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5910]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
Code information Lot Code: Model No. 7554; UDI-DI 00661392008342; Lot#6A3146, Expiration Date 01/22/2028 GTIN: (01)00661392008342(10)6A3146(17)280122
Distribution pattern US Nationwide distribution in the states of MD, IL, MN.
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[706]
FDA event record
· Exact recall-number query on openFDA
