Recall events
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Event 98234
Event summary
Timeline bucket December 26, 2025
Product types Device
Classifications Class II
Statuses Ongoing
Recalling firm wording GOLD STAR DISTRIBUTION 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
5 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 5
Bandages and first aid kits: FIRST AID KIT 24/42PC, LUCKY FIRST AID BANDAGES 24CT
Z-1180-2026
Recall number Z-1180-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity unknown
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Potential exposure of rodents and rodent activity in the distribution center.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Storage
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1180-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[11725]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
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Reason for recall Potential exposure of rodents and rodent activity in the distribution center.
Code information FIRST AID KIT 24/42PC, UPC 808829102536; LUCKY FIRST AID BANDAGES 24CT, UPC 808829041002. All codes purchased from this firm
Distribution pattern US Nationwide distribution in the states of Minnesota.
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[1453]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 5
Condoms, labeled as: TROJAN MAGNUM CONDOMS 6/DSP BLACK, TROJAN LUBRICATED CONDOMS 6/DSP LITE BLUE, TROJAN SPERMICIDE CONDOMS 6/DSP DARK BLUE, TROJAN ULTRA THIN CONDOMS 6/DSP GREY, TROJAN RIBBED CONDOMS 6/DSP GOLD/BROWN, TROJAN NONLUBRICATED CONDOMS 6/DSP RED, TROJAN ULTRA HER PLEASURE CONDOMS 6/DSP, TROJAN CONDOMS MAGNUM 48 CT DISP, *BOX TROJAN CONDOMS MAGNUM 50CT .
Z-1181-2026
Recall number Z-1181-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity unknown
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Potential exposure of rodents and rodent activity in the distribution center.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Storage
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1181-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[23423]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
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Reason for recall Potential exposure of rodents and rodent activity in the distribution center.
Code information TROJAN MAGNUM CONDOMS 6/DSP BLACK, UPC 022600642039; TROJAN LUBRICATED CONDOMS 6/DSP LITE BLUE, UPC 022600930501; TROJAN SPERMICIDE CONDOMS 6/DSP DARK BLUE, UPC 022600931508; TROJAN ULTRA THIN CONDOMS 6/DSP GREY, UPC 022600926207; TROJAN RIBBED CONDOMS 6/DSP GOLD/BROWN, UPC 022600940500; TROJAN NONLUBRICATED CONDOMS 6/DSP RED, UPC 22600920502; TROJAN ULTRA HER PLEASURE CONDOMS 6/DSP, UPC 022600973201; TROJAN CONDOMS MAGNUM 48 CT DISP, UPC 815556020125; *BOX TROJAN CONDOMS MAGNUM 50Ct, UPC none All codes purchased from this firm
Distribution pattern US Nationwide distribution in the states of Minnesota.
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[1169]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 5
Feminine hygiene products, labeled as: KOTEX FREEDOM MAXI NO WINGS 48CT, ALWAYS THIN LINERS UNSCENTED 12 CT, ALWAYS THIN LINERS SCENTED 12CT, ALWAYS ULT.THIN WINGS REG.12/22CT, ALWAYS ULT.THIN OVER NIGHT WINGS 12/16CT, JULIE MAXI NIGHT W.WINGS 36/10CT, STAY FREE REG. 12/10CT, STAY FREE SUPER 24/6CT, TAMPAX REG. 10CT, TAMPAX SUPER 10CT.
Z-1182-2026
Recall number Z-1182-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity unknown
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Potential exposure of rodents and rodent activity in the distribution center.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Storage
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1182-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5834]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
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Inspect official wording and provenance
Reason for recall Potential exposure of rodents and rodent activity in the distribution center.
Code information KOTEX FREEDOM MAXI NO WINGS 48CT, UPC 8935107214222; ALWAYS THIN LINERS UNSCENTED 12 CT, UPC 037000426882; ALWAYS THIN LINERS SCENTED 12CT, UPC 037000426899; ALWAYS ULT.THIN WINGS REG.12/22CT, UPC none; ALWAYS ULT.THIN OVER NIGHT WINGS 12/16CT, UPC none; JULIE MAXI NIGHT W.WINGS 36/10CT, UPC 710865100653; STAY FREE REG. 12/10CT, UPC 078300070320; STAY FREE SUPER 24/6CT, UPC 078300070245; TAMPAX REG. 10CT, UPC 073010214095; TAMPAX SUPER 10CT, UPC 073010314092. All codes purchased from this firm
Distribution pattern US Nationwide distribution in the states of Minnesota.
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[1292]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 5
Toothbrushes, labeled as: ORAL B TOOTH BRUSH SHINY CLEAN SOFT 12CT; COLGATE TOOTH BRUSH MED. 12CT; ADULT TOOTHPASTE W BRUSH (WHITENING) 6.4oz/24ct; ADULT TOOTHPASTE W BRUSH (ANTICAV) 6.4oz/24ct.
Z-1183-2026
Recall number Z-1183-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity UNKNOWN
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Potential exposure of rodents and rodent activity in the distribution center.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Storage
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1183-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[52783]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
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Compare all device evidence states
Inspect official wording and provenance
Reason for recall Potential exposure of rodents and rodent activity in the distribution center.
Code information ORAL B TOOTH BRUSH SHINY CLEAN SOFT 12CT, UPC 3014260786847; COLGATE TOOTH BRUSH MED. 12CT, UPC 6001067007289; ADULT TOOTHPASTE W BRUSH (WHITENING) 6.4oz/24ct, UPC 808829106879; ADULT TOOTHPASTE W BRUSH (ANTICAV) 6.4oz/24ct, UPC 808829106886. All codes purchased from this firm
Distribution pattern US Nationwide distribution in the states of Minnesota.
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[1338]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 5
PREGNANCY TEST 24CT
Z-1184-2026
Recall number Z-1184-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity N/A
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Potential exposure of rodents and rodent activity in the distribution center.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Storage
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1184-2026
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5838]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Potential exposure of rodents and rodent activity in the distribution center.
Code information UPC 048155920200
Distribution pattern US Nationwide distribution in the states of Minnesota.
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[1438]
FDA event record
· Exact recall-number query on openFDA
