Recall events
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Event 93216
Event summary
Timeline bucket October 04, 2023
Product types Device
Classifications Class II
Statuses Ongoing
Recalling firm wording Family Dollar Stores, Llc.
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
10 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 10
CLEARBLUE SMART COUNTDOWN PRGNCY TST 1CT, SKU 900260
Z-0261-2024
Recall number Z-0261-2024
Initiated October 04, 2023
Classification Class II
Status Ongoing
Quantity 329,044 total units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products were stored outside of labeled temperature requirements.
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-0261-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[57422]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products were stored outside of labeled temperature requirements.
Code information All units sold at stores between June 1, 2023 and October 4, 2023.
Distribution pattern Distributed to Family Dollar stores in the following states: GA, AL, MS, FL, LA, AR, AZ, KS, TX, OK, CO, NM, NE, UT, NV, WY, ID, SD, ND, CA, MT, OR, WA.
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[6451]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 10
AT HOME MARIJUANA TEST STRIP, SKU 900752
Z-0262-2024
Recall number Z-0262-2024
Initiated October 04, 2023
Classification Class II
Status Ongoing
Quantity 329,044 total units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products were stored outside of labeled temperature requirements.
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-0262-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[34804]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products were stored outside of labeled temperature requirements.
Code information All units sold at stores between June 1, 2023 and October 4, 2023.
Distribution pattern Distributed to Family Dollar stores in the following states: GA, AL, MS, FL, LA, AR, AZ, KS, TX, OK, CO, NM, NE, UT, NV, WY, ID, SD, ND, CA, MT, OR, WA.
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[6471]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 10
FIXODENT ORG CREAM 2.4OZ, SKU 906018 FIXODENT ADH CREAM WITH SCOPE 2OZ, SKU 906402 FIXODENT ORG CREAM TRAVEL .75OZ, SKU 901239
Z-0263-2024
Recall number Z-0263-2024
Initiated October 04, 2023
Classification Class II
Status Ongoing
Quantity 329,044 total units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products were stored outside of labeled temperature requirements.
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-0263-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5035]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products were stored outside of labeled temperature requirements.
Code information All units sold at stores between June 1, 2023 and October 4, 2023.
Distribution pattern Distributed to Family Dollar stores in the following states: GA, AL, MS, FL, LA, AR, AZ, KS, TX, OK, CO, NM, NE, UT, NV, WY, ID, SD, ND, CA, MT, OR, WA.
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[6568]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 10
VERIQUICK PREGNANCY TEST 1CT, SKU 901260
Z-0264-2024
Recall number Z-0264-2024
Initiated October 04, 2023
Classification Class II
Status Ongoing
Quantity 329,044 total units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products were stored outside of labeled temperature requirements.
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-0264-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[16786]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products were stored outside of labeled temperature requirements.
Code information All units sold at stores between June 1, 2023 and October 4, 2023.
Distribution pattern Distributed to Family Dollar stores in the following states: GA, AL, MS, FL, LA, AR, AZ, KS, TX, OK, CO, NM, NE, UT, NV, WY, ID, SD, ND, CA, MT, OR, WA.
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[6988]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 10
DENTEMP ONE STEP .077OZ, SKU 902139
Z-0265-2024
Recall number Z-0265-2024
Initiated October 04, 2023
Classification Class II
Status Ongoing
Quantity 329,044 total units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products were stored outside of labeled temperature requirements.
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-0265-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[9696]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products were stored outside of labeled temperature requirements.
Code information All units sold at stores between June 1, 2023 and October 4, 2023.
Distribution pattern Distributed to Family Dollar stores in the following states: GA, AL, MS, FL, LA, AR, AZ, KS, TX, OK, CO, NM, NE, UT, NV, WY, ID, SD, ND, CA, MT, OR, WA.
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[6563]
FDA event record
· Exact recall-number query on openFDA
device · product 6 of 10
FIRST RESPONSE 2 CT, SKU 902343
Z-0266-2024
Recall number Z-0266-2024
Initiated October 04, 2023
Classification Class II
Status Ongoing
Quantity 329,044 total units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products were stored outside of labeled temperature requirements.
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-0266-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5031]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products were stored outside of labeled temperature requirements.
Code information All units sold at stores between June 1, 2023 and October 4, 2023.
Distribution pattern Distributed to Family Dollar stores in the following states: GA, AL, MS, FL, LA, AR, AZ, KS, TX, OK, CO, NM, NE, UT, NV, WY, ID, SD, ND, CA, MT, OR, WA.
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[6430]
FDA event record
· Exact recall-number query on openFDA
device · product 7 of 10
GOODSENSE DENTURE CLEANSER GRN TAB 40CT, SKU 906312 GOODSENSE DENTURE CLEAN OVRNT TAB 40CT, SKU 906023
Z-0267-2024
Recall number Z-0267-2024
Initiated October 04, 2023
Classification Class II
Status Ongoing
Quantity 329,044 total units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products were stored outside of labeled temperature requirements.
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-0267-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5039]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products were stored outside of labeled temperature requirements.
Code information All units sold at stores between June 1, 2023 and October 4, 2023.
Distribution pattern Distributed to Family Dollar stores in the following states: GA, AL, MS, FL, LA, AR, AZ, KS, TX, OK, CO, NM, NE, UT, NV, WY, ID, SD, ND, CA, MT, OR, WA.
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[6469]
FDA event record
· Exact recall-number query on openFDA
device · product 8 of 10
ARC TEETH WHITENING PEN 0.06 FL OZ, SKU 997950
Z-0268-2024
Recall number Z-0268-2024
Initiated October 04, 2023
Classification Class II
Status Ongoing
Quantity 329,044 total units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products were stored outside of labeled temperature requirements.
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-0268-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[34802]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products were stored outside of labeled temperature requirements.
Code information All units sold at stores between June 1, 2023 and October 4, 2023.
Distribution pattern Distributed to Family Dollar stores in the following states: GA, AL, MS, FL, LA, AR, AZ, KS, TX, OK, CO, NM, NE, UT, NV, WY, ID, SD, ND, CA, MT, OR, WA.
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[6266]
FDA event record
· Exact recall-number query on openFDA
device · product 9 of 10
MEDIC's CHOICE CONTACT LENS SOLUTION 12FLOZ, SKU 998935
Z-0269-2024
Recall number Z-0269-2024
Initiated October 04, 2023
Classification Class II
Status Ongoing
Quantity 329,044 total units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products were stored outside of labeled temperature requirements.
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-0269-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[28536]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products were stored outside of labeled temperature requirements.
Code information All units sold at stores between June 1, 2023 and October 4, 2023.
Distribution pattern Distributed to Family Dollar stores in the following states: GA, AL, MS, FL, LA, AR, AZ, KS, TX, OK, CO, NM, NE, UT, NV, WY, ID, SD, ND, CA, MT, OR, WA.
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[6515]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-0270-2024
Initiated October 04, 2023
Classification Class II
Status Ongoing
Quantity 329,044 total units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Products were stored outside of labeled temperature requirements.
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-0270-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[46323]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Products were stored outside of labeled temperature requirements.
Code information All units sold at stores between June 1, 2023 and October 4, 2023.
Distribution pattern Distributed to Family Dollar stores in the following states: GA, AL, MS, FL, LA, AR, AZ, KS, TX, OK, CO, NM, NE, UT, NV, WY, ID, SD, ND, CA, MT, OR, WA.
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[6302]
FDA event record
· Exact recall-number query on openFDA
