The Recall Desk

State

Georgia product recalls

20,371 recalls have nationwide distribution and so reach Georgia. 0 additional recalls listed Georgia specifically in their distribution scope.

About recalls in Georgia

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Georgia consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

15876–15900 of 20371

  • HighFDA (Devices)·Z-1579-2022·2022-08-31

    Baxter Syringe Tip Caps Recalled for Potential Sterile Barrier Failure

    Baxter Healthcare Corporation is recalling 168,390 units of DISCPAC Syringe Tip Caps because the packaging may not maintain a sterile barrier, creating a contamination risk.

    Product
    Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Green: a) 25 pack, REF H93869025, b) 100 pack, REF H938674100, c) 100 pack, REF H93869100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1401-2022·2022-08-31

    Jet Alert Tablets Recalled for Improper Storage Temperature Conditions

    Jet Alert stimulant tablets distributed nationwide from April to June 2022 are being recalled due to improper storage temperature conditions that may affect product safety and efficacy.

    Product
    JET ALERT TABLET 30 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1373-2022·2022-08-31

    Multiple ibuprofen products recalled for improper storage temperature

    Family Dollar is recalling multiple ibuprofen products, including MOTRIN and GOOD SENSE brands, due to improper storage temperature conditions at distribution facilities from April through June 2022.

    Product
    MOTRIN IB CAPLETS 24CT SKU999394; GOOD SENSE IBUPROFEN 200MG TABLETS 24CT SKU 900556;GOOD SENSE IBUPROFEN 200MG CAPLET 50 CT SKU 902333 MOTRIN CHILDREN'S BUBBLEGUM 4 FL OZ SKU 903048 GOOD SENSE IBUPROFEN REGULAR SOFTGELS 160CT SKU 999373 GOOD SENSE IBUPROFEN 200 MG CAPLE
    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. Alere
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1411-2022·2022-08-31

    Swan Calamine Lotion Nationwide Recall for Temperature Storage Deviations

    Family Dollar Stores is recalling Swan Calamine Lotion 6 FL OZ due to CGMP deviations involving improper storage temperature. No illnesses or injuries have been reported.

    Product
    SWAN CALAMINE LOTION 6 FL OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1622-2022·2022-08-31

    Dynarex Nail Polish Remover Pads Recalled for Reduced Effectiveness from Heat Exposure

    Mckesson Medical-Surgical Inc. is recalling Dynarex Nail Polish Remover Pads due to facility temperature excursions in summer 2021 that may have reduced product effectiveness. All lots received between June 1 and September 30, 2021, nationwide are affected.

    Product
    Dynarex¿ PAD, NAIL POLISH REMOVER (100/BX 10BX/CS) DYNREX Catalog # 1501
    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
  • 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-1406-2022·2022-08-31

    Baby Cough Medicine Recalled for Improper Storage Temperature

    Zarbee's Naturals baby cough syrup has been recalled due to storage temperature deviations at Family Dollar stores between April and June 2022.

    Product
    ZARBEES NTRLS BABY CGH MUCUS GRP 2 FL OZ 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-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 (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-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 (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
  • ModerateFDA (Devices)·Z-1587-2022·2022-08-31

    McKesson Pregnancy Test Kits Recalled for Temperature Exposure During Storage

    McKesson recalls hCG pregnancy test kits nationwide due to facility temperature excursions that may have compromised product effectiveness. Affected lots were received between June and September 2021.

    Product
    a. McKesson Rapid Test Kit McKesson Consult Fertility Test hCG Pregnancy Test Serum / Urine Sample 25 Tests. Model Number: 5002. b. McKesson Consult Rapid Test Kit McKesson Consult Fertility Test hCG Pregnancy Test Urine Sample 25 Tests Model Number: 5000. c. McKesso
    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-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 thro
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1569-2022·2022-08-31

    Anatomical Model Recalled for Wrong Product Shipped in Packaging

    Materialise USA LLC is recalling ProPlan CMF Anatomical Model units where packages labeled MU22-INA-DUQ contained the wrong anatomical model inside. Recipients should verify their package contents match the label.

    Product
    ProPlan CMF Anatomical Model, Maxilla-Cranium, Clear Identification number SD900.208
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1433-2022·2022-08-31

    Acne Treatment Products Recalled for Improper Storage Conditions

    Family Dollar Stores is recalling two acne treatment products due to storage condition deviations. The products were held outside appropriate temperature ranges.

    Product
    ACNE FREE ADAPALENE GL ACN TRTMT 0.5 OZ SKU 2096518 ACNE FREE TRMINTR 10 SPOT TRTMT 1 OZ SKU 2096507 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1378-2022·2022-08-31

    Antibacterial Wipes Recalled for Improper Storage Conditions

    Family Dollar Stores recalls Disney Licensed Anti Bac Wipes and Antibacterial Wipes due to storage temperature deviations. The products were distributed nationwide to Family Dollar stores from April 30 through June 10, 2022.

    Product
    DISNEY LICENSED ANTI BAC WIPES 20 CT SKU 998908; ANTIBACTERIAL WIPES 40CT SKU 2007538 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1456-2022·2022-08-31

    OTC Cough Medications Recalled for Improper Storage Temperature

    Family Dollar is recalling four OTC cough and mucus relief medications that were stored outside appropriate temperature conditions.

    Product
    REFENESEN MUCUS RELIEF TABLET 30 CT SKU 917531 MUCINEX DM MAX STRENGTH 7CT SKU 900854 RIC MUCUS RLF DM MAX STNGTH CHRY 6FL OZ SKU 999559 VICKS JARABE COUGH CONGESTION 8FLOZ SKU 998933 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1460-2022·2022-08-31

    Mucinex SE Max Strength recalled for improper storage conditions

    Family Dollar Stores is recalling Mucinex SE Max Strength 7CT distributed from April through June 2022 due to CGMP deviations involving improper storage temperature.

    Product
    MUCINEX SE MAX STRENGTH 7CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • 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 BAYER
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1422-2022·2022-08-31

    Ready In Case Isopropyl Alcohol Products Recalled for Storage Temperature Deviation

    Family Dollar Stores is recalling Ready In Case rubbing alcohol and isopropyl alcohol products due to improper storage temperature conditions. The recall affects four SKUs distributed nationwide.

    Product
    READY IN CASE RUBBING ALCOHOL 91 PCT 16 FL OZ SKU 902270 READY IN CASE 70 PCT ISOPROPYL ALCOHOL 32 FL OZ SKU 999747 READY IN CASE 91PCT ISOPROPYL ALCOHOL 32 FL OZ SKU 999742 READY IN CASE 70PCT ISOPROPYL ALCOHOL 16 FL OZ SKU 999743 distributed to specific Family Dollar Stor
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1377-2022·2022-08-31

    Dial Men's Eucalyptus Body Wash Recalled Due to Storage Temperature Deviation

    Family Dollar Stores is recalling Dial Men's Eucalyptus Body Wash 20 fl oz due to improper storage temperature conditions during distribution.

    Product
    DIAL MENS EUCALYPTUS AB BODY WASH 20 FLOZ SKU 2096030 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Consumer Product
    Distribution
    Distributed nationwide