The Recall Desk

State

North Dakota product recalls

73,388 recalls have nationwide distribution and so reach North Dakota. 2,924 additional recalls listed North Dakota specifically in their distribution scope.

What the numbers show

Total
2,924
Critical
265
Severe
869
Most recent
2026-09-23

Of the 2,924 recalls naming North Dakota we have scored against our rubric, 265 (9%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 869 (30%) are Severe.

Which agencies issued them

These figures cover only the 2,924 recalls whose distribution notice names North Dakota specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19901–19925 of 76312

  • ModerateFDA (Drugs)·D-1424-2022·2022-08-31

    Aspirin Products Recalled Due to Improper Storage Conditions at Family Dollar

    Multiple aspirin products sold at Family Dollar Stores have been recalled due to storage temperature deviations during distribution from April 30 through June 10, 2022.

    Product
    FW ASPIRIN CHEWABLE TABLET 36CT SKU 913990 GS ENTERIC ASPIRIN TABLET 120 CT SKU 913724 BAYER BACK BODY EX STRGTH CAPLETS 24CT SKU 900438 BAYER LOW DOSE 81 MG TABLET 120 CT SKU 916070 BAYER ASPIRIN 325MG TABLET 24CT SKU 913996 BAYER LOW DOSE TABLET 32CT SKU 915641…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1598-2022·2022-08-31

    Strep A Test Kits Recalled for Potential Temperature Damage

    Multiple Strep A diagnostic test kits are being recalled due to temperature exposure during manufacturing and storage that may have compromised test accuracy. All lots received between June 1 and September 30, 2021 are affected.

    Product
    Strep test: a. McKesson Medical-Surgical McKesson Rapid Test Kit McKesson Consult Infectious Disease Immunoassay Strep A Test Throat / Tonsil Saliva Sample 25 Tests, Model Number: 5003. b. QUIDEL Sofia TEST KIT, STREP A+ SOFIA (25/KT 12KT/CS) Model Number: 20274. c.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1446-2022·2022-08-31

    Excedrin Migraine Caplets Recalled Due to Improper Storage Conditions

    Family Dollar Stores is recalling Excedrin Migraine Caplets (24 CT) due to improper storage temperature conditions that may affect product quality. Affected products were distributed nationwide between April 30 and June 10, 2022.

    Product
    EXCEDRIN MIGRAINE CAPLET 24 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1599-2022·2022-08-31

    Merit Medical Systems Aspira Kits Recalled Due to Temperature Excursions

    Merit Medical Systems Aspira Dressing and Drainage Kits recalled due to facility temperature excursions from June to August 2021. Exposure to higher temperatures may have reduced product effectiveness; no illnesses reported.

    Product
    a. MERIT MEDICAL SYSTEMS Aspira Dressing Kit Aspira Model Number: 4991503. b. MERIT MEDICAL SYSTEMS Aspira Pleural / Peritoneal Drainage Kit Aspira 1000 mL Sterile Model Number: 4992301.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1389-2022·2022-08-31

    Lidocaine arthritis topical product recalled due to improper storage

    Family Dollar Stores is recalling Lidocaine Arthritis and Sport wintergreen liniment (16 fl oz, SKU 902929) distributed nationwide April 30–June 10, 2022, due to improper storage temperature conditions.

    Product
    LIDOCAINE ARTHRITIS AND SPORT WNTGRN 16 FLOZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1428-2022·2022-08-31

    Fleet Glycerin Suppositories Recalled for Storage Temperature Violations

    Fleet Glycerin Suppositories distributed nationwide from April 30 to June 10, 2022, are being recalled because the product was held outside appropriate storage temperature conditions.

    Product
    FLEET GLYCERIN SUPPOSITORIES 50 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1415-2022·2022-08-31

    Alka Seltzer Extra Strength 24 CT Recalled for Improper Storage Conditions

    Family Dollar Stores is recalling Alka Seltzer Extra Strength 24 CT due to products stored outside proper temperature conditions, which may affect product quality.

    Product
    ALKA SELTZER EXTRA STRENGTH 24 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1435-2022·2022-08-31

    Four Topical Analgesic Products Recalled for Improper Storage Conditions

    Four topical analgesic products distributed to Family Dollar stores were recalled due to CGMP violations involving improper storage temperature conditions. No illnesses or injuries have been reported.

    Product
    ARTHRITIS HOT CREME 3 OZ SKU 901452 ICY HOT PATCH 1 CT SKU 911030 ICY HOT MUSCLE RUB 1.25 OZ SKU 920205 ICY HOT NO MESS 1.5 OZ SKU 998751 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1417-2022·2022-08-31

    Omeprazole Tablets Recalled Due to Improper Storage Conditions

    Good Sense and Prilosec OTC omeprazole tablets distributed by Family Dollar Stores have been recalled due to improper storage temperature conditions. No illnesses have been reported.

    Product
    GOOD SENSE OMEPRAZOLE TABLET 14CT SKU 900055 PRILOSEC OTC TABLET 14 CT SKU914128 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1636-2022·2022-08-31

    Fisher Scientific Swabs Recalled for Temperature Excursion During Storage

    Mckesson Medical-Surgical Inc. is recalling Fisherbrand laboratory swabs due to facility temperature excursions from June through August 2021 that may have impacted product effectiveness. All affected lots distributed between June 1 and September 30, 2021 are included.

    Product
    FISHER SCIENTIFIC Fisherbrand SWAB, ROUND BOTTOM CLR (50/PK)FSHSCI Catalog # 1490712
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1396-2022·2022-08-31

    Preferred Urinary Pain Relief Product Recalled for Improper Storage Conditions

    Family Dollar Stores is recalling Preferred Urinary Pain Relief Max Strength due to CGMP violations involving improper storage temperature. Product was distributed nationwide April 30 through June 10, 2022.

    Product
    PREFERRED URINRY PN RLF MAX STRNGTH 12 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1421-2022·2022-08-31

    RIC Stool Softener Recalled Due to Storage Temperature Deviations

    RIC Stool Softener Softgels (SKUs 917000 and 902493) distributed to Family Dollar Stores nationwide from April 30, 2022 through June 10, 2022 are recalled due to improper storage temperature conditions.

    Product
    RIC STOOL SOFTENER SOFTGEL 100 CT SKU 917000 RIC STOOL SOFTNER 100 CT SKU 902493 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1434-2022·2022-08-31

    Voltaren Arthritis Pain Gel Recalled for Improper Storage Conditions

    Family Dollar Stores is recalling Voltaren Arthritis Pain Gel 20G distributed April–June 2022 due to storage temperature deviations that may affect product effectiveness.

    Product
    VOLTAREN ARTHRITIS PAIN GEL 20G distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1618-2022·2022-08-31

    BD Vacutainer Blood Collection Tubes Recalled for Temperature-Exposure Effectiveness Loss

    BD Vacutainer blood collection tubes are recalled due to potential temperature damage during storage from June to August 2021. Affected tubes received between June 1 and September 30, 2021 may have reduced effectiveness.

    Product
    a. BECTON DICKINSON BD Vacutainer SST TUBE, BLD COL CLOT/SEP GLD 3.5ML PLAS VACUTAINER (100/BX), Model Number: 367983. b. BECTON DICKINSON BD Vacutainer SST TUBE, BLD COL CLOT/SEP RED/GRY8.5ML PLAS VACUTAINER (100/BX Model Number: 367988. c. BECTON DICKINSON BD…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1440-2022·2022-08-31

    NPX Enema 4.5 FL OZ Two-Pack Recalled for Improper Storage

    Family Dollar Stores is recalling NPX Enema 4.5 FL OZ 2-packs due to improper storage conditions that violate manufacturing standards. The product was held outside appropriate temperature conditions at select Family Dollar stores between April 30 and June 10, 2022.

    Product
    NPX ENEMA 4.5 FL OZ 2 PK distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1637-2022·2022-08-31

    Total-Fix parasitology stool collection kit recalled for temperature exposure

    Mckesson is recalling a Total-Fix stool collection parasitology kit due to temperature exposure that may have reduced its effectiveness. All lots received between June 1 and September 30, 2021 are affected.

    Product
    MEDICAL CHEMICAL CORPORATION Total-Fix STOOL COLL KIT, TOTAL FIX PARASITOLOGY (100/CS) Catalog # NC0585129
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1375-2022·2022-08-31

    Antifungal spray and powder recalled for improper storage temperature conditions

    Family Dollar Stores recalled two antifungal products due to storage temperature deviations. The products may have been compromised in effectiveness due to failure to maintain proper storage conditions.

    Product
    DR SCHOLLS ANTI FUNGAL SPRAY PWDER 4.7 OZ SKU 998250 PREMIER ANTFGL TLNFTT LQ SPRY 5.3 FL OZ SKU 911077 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·028-2022·2022-08-30

    Connoisseur’s Kitchen Recalls Imported Frozen Chicken Entrees Over Listeria Risk

    Connoisseur’s Kitchen is recalling approximately 880 pounds of imported frozen ready-to-eat chicken entrees due to possible Listeria monocytogenes contamination. No illnesses have been reported.

    Product
    Connoisseur’s Kitchen Recalls Imported Frozen Chicken Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E073000·2022-08-30

    Oshkosh Recalls Shepphard Steering Gears for S-Series 2.0 Vehicles

    Oshkosh is recalling certain Shepphard steering gears for S-Series 2.0 vehicles because incorrect assembly may cause the gear to fracture, potentially leading to a loss of steering control.

    Product
    STEERING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V655000·2022-08-30

    Motorhomes with improperly routed hydraulic lines pose fire risk

    REV is recalling 2018-2023 motorhome models from Fleetwood and Holiday Rambler because hydraulic lines may be improperly routed or protected, risking fluid leaks that could cause fires. Dealers will repair free of charge.

    Product
    HOLIDAY RAMBLER — HOLIDAY RAMBLER, FLEETWOOD VESTA, JAMBOREE, ADMIRAL, FLAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V656000·2022-08-30

    Porsche Recalls Vehicles for Missing Headlight Adjustment Caps

    Porsche is recalling 2001-2020 models because missing caps on headlight adjustment screws can cause improper alignment, increasing crash risk.

    Product
    PORSCHE — PORSCHE CAYENNE TRANSSYBERIA, CAYENNE, PANAMERA, BOXSTER S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V650000·2022-08-29

    Tiffin Wayfarer Motorhomes Recalled for Loose Wheel Lug Nuts

    Wayfarer is recalling 2017-2020 Tiffin Wayfarer motorhomes because wheel lug nuts may not have been properly tightened during a previous repair, posing a crash risk.

    Product
    TIFFIN — TIFFIN WAYFARER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V652000·2022-08-29

    Audi Recalls 2022 A3, S3, and RS3 Models for Air Bag Defect

    Volkswagen Group of America is recalling 2022 Audi A3, S3, and RS3 vehicles because the front passenger air bag may be folded incorrectly, increasing injury risk in a crash.

    Product
    AUDI — AUDI A3, S3, RS 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V654000·2022-08-29

    Western Star 47X and 49X commercial trucks recalled for detaching hood bezel covers

    Daimler Trucks North America is recalling certain 2020-2023 Western Star 47X and 49X commercial trucks because hood bezel covers may detach, creating a road hazard and increasing crash risk. Approximately 3,498 vehicles are affected.

    Product
    WESTERN STAR — WESTERN STAR 49X, 47X
    Category
    Vehicle
    Distribution
    Distributed nationwide