State

Arkansas product recalls

73,388 recalls have nationwide distribution and so reach Arkansas. 5,542 additional recalls listed Arkansas specifically in their distribution scope.

What the numbers show

Total: 5,542
Critical: 1,029
Severe: 1,446
Most recent: 2026-09-23

Of the 5,542 recalls naming Arkansas we have scored against our rubric, 1,029 (19%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,446 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,542 recalls whose distribution notice names Arkansas specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20276–20300 of 78930

HighFDA (Devices)·Z-1590-2022·2022-08-31
Alcon Contact Lens Solutions Recalled for Temperature Exposure During Storage and Transit
Multiple Alcon contact lens solutions were recalled due to facility temperature excursions during storage and transit that may have reduced product effectiveness. Affected products include Clear Care and Opti Free Replenish solutions distributed nationwide between June and September 2021.
Product
a. Alcon Clear Care Contact Lens Solution Clear Care 12 oz. Solution, Model Number: 65035820, Model Number: USSCupA-12BUP300. b. Alcon Contact Lens Solution Opti Free Replenish 4 oz. Solution Model Number: 00065035604 Model Number: USSCupA-12BUP300. c. Alcon Contact…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1595-2022·2022-08-31
Cadwell Disposable Ground Electrodes Recalled Due to Temperature Exposure
Cadwell Disposable Ground Electrodes may have reduced effectiveness due to facility temperature excursions between June and August 2021. All units distributed nationwide received between June 1 and September 30, 2021 are affected.
Product
Cadwell Disposable Ground Electrodes Grounding Pad 1.25 X 1.75 Inch Dimensions, Disposable Model Number: 302288-000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1580-2022·2022-08-31
Baxter Syringe Tip Caps Recalled Due to Sterile Packaging Barrier Risk
Baxter Healthcare is recalling DISCPAC Syringe Tip Caps because the packaging may not maintain a sterile barrier. The product was distributed nationwide and internationally.
Product
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Pink, 100 pack, REF H938676100
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1577-2022·2022-08-31
Baxter DISCPAC Syringe Tip Caps recalled for packaging sterility concerns
Baxter Healthcare is recalling DISCPAC Syringe Tip Caps due to potential packaging failures that could compromise the sterile barrier on 10,140 units distributed worldwide.
Product
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, White REF H938671100
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1444-2022·2022-08-31
AFRIN No Drip Severe Congestion Recalled for Improper Storage Temperature
Family Dollar Stores is recalling AFRIN No Drip Severe Congestion 0.5 FL oz due to improper storage temperature conditions (CGMP deviation). The product was distributed to specific Family Dollar locations from April 30 through June 10, 2022.
Product
AFRIN NO DRIP SEVERE CONGESTION 0.5FL OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·22V660000·2022-08-31
2022 Nissan Rogue Fuel Tank May Leak Following Modifications
Certain 2022 Nissan Rogue vehicles have fuel tanks that may have been punctured during vehicle modifications, creating potential fuel leak and fire risk. Nissan will inspect and replace affected fuel tanks free of charge.
Product
NISSAN — NISSAN redundant ROGUE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1615-2022·2022-08-31
MedSource IV Start Kit Recalled for Temperature-Related Effectiveness Loss
McKesson is recalling MedSource IV Start kits due to facility temperature excursions that may have compromised product effectiveness. Affected units were received between June and September 2021.
Product
MedSource IV Start kit, 8inch Extension Set IV START KIT, W/SITE LOC/8" EX100/CS Model Number: MS-80047
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1581-2022·2022-08-31
Baxter DISCPAC Syringe Tip Caps Recalled for Potential Sterile Barrier Failure
Baxter is recalling DISCPAC Syringe Tip Caps due to potential packaging defect that may not maintain sterile barrier. The recall affects 8,500 units distributed worldwide.
Product
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Purple, 100 pack, REF H938677100
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1366-2022·2022-08-31
Personal Care Lotions Recalled Due to Improper Storage Temperature
Family Dollar Stores is recalling multiple lotion products that were held outside appropriate storage temperatures. The affected brands include Dermasil, Aveeno, and Vaseline products distributed from April 30 through June 10, 2022.
Product
Dermasil Dry Skin Treatment 10 OZ SKU 2098068 Aveeno Daily Moisturizing Lotion 5 OZ SKU 2005444 Aveeno Baby Daily Moistue Lotion 8 OZ SKU 900016 Vaseline Mens Extra Strength Body and Face Lotion 10 OZ SKU 2003674 distributed to specific Family Dollar Stores 04/30/2022…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1410-2022·2022-08-31
Swan Povidone 4 FL OZ Recalled for Improper Storage Temperature
Family Dollar Stores recalled Swan Povidone 4 FL OZ due to storage temperature deviations that may affect product quality. Products distributed nationwide from April to June 2022 should not be used.
Product
SWAN POVIDONE 4 FL OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1436-2022·2022-08-31
Lidocaine Cream Products Recalled for Improper Storage Conditions at Family Dollar
Family Dollar is recalling Aspercreme with Lidocaine Creme (SKU 999852) and Icy Hot Lidocaine Cream (SKU 999853) distributed April 30 through June 10, 2022 nationwide due to improper storage temperature conditions.
Product
ASPERCREME WITH LIDOCAINE CREME 1.75 OZ SKU 999852 ICY HOT LIDOCAINE CREAM 1.75 OZ SKU 999853 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1409-2022·2022-08-31
Doctor Teal's Epsom Salt Recalled for Improper Storage Conditions
Family Dollar Stores is recalling Doctor Teal's Pure Epsom Salt packages distributed April 30–June 10, 2022 due to improper storage temperature conditions.
Product
DOCTOR TEALS PURE EPSOM SALT UNSCENTED 6 LBS SKU 999355 Ready in case EPSOM SALTS 2 LB SKU 909223 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1419-2022·2022-08-31
PEPCID antacid tablets recalled for improper storage temperature handling
Family Dollar Stores is recalling three PEPCID antacid products due to improper storage temperature conditions at specific Family Dollar locations from April through June 2022.
Product
PEPCID COMPLETE CHEWABLE TAB BERRY 8CT SKU 903365 PEPCID AC MAXIMUM STRENGTH TABLET 25 CT SKU 902063 PEPCID AC MAXIMUM STRENGTH TABLET 8 CT SKU 914773 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1589-2022·2022-08-31
Drugs of Abuse Test Kits Recalled Due to Temperature Exposure
McKesson Medical-Surgical is recalling multiple brands of drugs of abuse test kits because temperature excursions prior to delivery may have reduced product effectiveness.
Product
Drugs of Abuse Tests: a. Wondfo Tdip Drugs of Abuse Test Tdip Single Drug Fentanyl (FEN) Urine Sample 25 Tests. Model Number: AWFTY-114. b. Alere Drugs of Abuse Test E-Z Split Key Cup 12-Drug Panel AMP, BAR, BUP, BZO, COC, mAMP/MET, MDMA, MOP, MTD, OXY, PPX, THC Urine…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1385-2022·2022-08-31
Benadryl Extra Strength Cream Recalled for Improper Storage Conditions
Family Dollar Stores is recalling Benadryl Extra Strength Cream 1 oz distributed from April 30 through June 10, 2022, because the product was held outside appropriate storage temperature conditions. No illnesses have been reported.
Product
BENADRYL EXTRA STRENGTH CREAM 1 OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1416-2022·2022-08-31
Mylanta Max Strength Classic flavor antacid recalled for improper storage conditions
Mylanta Max Strength Classic flavor antacid (12 fl oz, SKU 999844) has been recalled due to improper storage temperature conditions. The product was distributed nationwide to Family Dollar Stores from April 30 to June 10, 2022.
Product
MYLANTA MAX STRENGTH CLASSIC FLVR 12 FLOZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1425-2022·2022-08-31
Family Dollar Laxative Products Recalled for Improper Storage Conditions
Family Dollar recalls two bisacodyl laxative products (SKUs 902449 and 915221) distributed to specific stores from April to June 2022 due to storage temperature deviations affecting product quality.
Product
QP LAXATIVE BISACODYL 5 MG TABLET 50 CT SKU 902449 QP WOMEN LAXATIVE BISCODYL TABLET 25 CT SKU 915221 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1407-2022·2022-08-31
Good Sense Hemorrhoid Products Recalled for Improper Storage Conditions
Good Sense Hemorrhoid Ointment and Wipes sold at Family Dollar stores from April through June 2022 are being recalled due to storage outside appropriate temperature conditions. No illnesses have been reported.
Product
GOOD SENSE HEMORRHOID OINTMENT 2 OZ SKU 910325 GOOD SENSE HEMORRHOIDAL WIPES 48 CT SKU 902260 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1380-2022·2022-08-31
Orajel Cold Sore Pain Cream Recalled for Improper Storage Conditions
Orajel Cold Sore Pain Cream 1.25 fl. oz. was recalled because it was stored outside appropriate temperature conditions. The product was distributed to Family Dollar Stores from April 30 through June 10, 2022.
Product
Orajel Cold Sore Pain Cream 1.25 fl. oz. distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1596-2022·2022-08-31
FDA Recalls Heparin Sodium Prefilled Syringes Due to Heat Damage
Mckesson Medical-Surgical Inc. is recalling Excelsior Heparin Sodium prefilled syringes that may have been damaged by temperature excursions during manufacturing, potentially affecting their effectiveness. The recall covers lots received between June and September 2021.
Product
Excelsior Heparin Sodium, Porcine, Preservative Free 100 U / mL Solution Prefilled Syringe, Partial Fill 5 mL Fill in 10 mL Syringe Model Number: 513604
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1611-2022·2022-08-31
IV Securement Kit Recall Due to Storage Temperature Damage
McKesson is recalling Medline Centurion IV Securement Kits that were exposed to high temperatures during storage, which may have impacted product effectiveness. No illnesses have been reported.
Product
MEDLINE INDUSTRIES Centurion IV Securement Kit Model Number: IVSSTK3
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1445-2022·2022-08-31
Nicorette Gum Recalled Due to Improper Storage Temperature Conditions
Family Dollar Stores is recalling NICORETTE GUM WHITE ICE MINT 4 MG distributed from April 30 through June 10, 2022. The product was held outside appropriate storage temperature conditions.
Product
NICORETTE GUM WHITE ICE MINT 4 MG 20 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1461-2022·2022-08-31
QP Cough Cold Tablets Recalled for Improper Storage Conditions
QP Cough Cold Tablet 16 CT units distributed to specific Family Dollar Stores nationwide are being recalled due to storage temperature deviations. No illnesses or injuries have been reported.
Product
QP COUGH COLD TABLET 16 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1612-2022·2022-08-31
Fischer Cone Biopsy Excisor recalled for potential temperature damage
McKesson is recalling Fischer Cone Biopsy Excisor Model 900-157 units because temperature excursions during storage may have compromised product effectiveness.
Product
Fischer Cone Biopsy Excisor EXCISOR, CONE FISCHER BIOPSY WD ANGL SM (5/BX) Model Number: 900-157
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1451-2022·2022-08-31
CLARITIN Allergy Products Recalled Due to Improper Storage Conditions
Family Dollar Stores is recalling specific CLARITIN allergy products (liquids and tablets) distributed from April through June 2022 due to improper storage temperature conditions that may affect product quality.
Product
CLARITIN ALLERGY LIQ CHLDRNS GRAPE 2 FLOZ SKU 900834 CLARITIN ALLERGY 10MG TABLETS 5 CT SKU 916116 GS ALLERGY LORATADINE TABLET 30 CT SKU 916114 CLARITIN ALLERGY 10 MG TABLET 10 CT SKU 901655 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide