The Recall Desk

Severity 2 of 5

Moderate recalls

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

What “moderate” means here

Severity 2 (Moderate) recalls cover minor labeling errors, low-risk contamination, and voluntary precautionary recalls. The agency's own classification is typically FDA Class III, or the issue is something like incomplete instructions or a small UPC mismatch where the product itself is safe but doesn't meet documentation requirements. Use the same brand-name product safely; follow the manufacturer's instructions for return or exchange if you want a refund.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

4276–4300 of 21589

  • ModerateFDA (Drugs)·D-1412-2022·2022-08-31

    Good Sense Sore Throat Spray Recalled for Improper Storage Conditions

    Family Dollar Stores recalls Good Sense Sore Throat Spray Cherry 6 FL OZ due to CGMP deviations involving improper storage temperature conditions. The product was distributed nationwide from April 30, 2022 through June 10, 2022.

    Product
    GOOD SENSE SORE THROAT SPRAY CHERRY 6 FL OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1633-2022·2022-08-31

    Dynarex Cotton Swabs Recalled Due to Temperature Exposure

    Mckesson Medical-Surgical is recalling Dynarex cotton swabs (197 boxes) received June 1–September 30, 2021, due to temperature excursions during storage that may have reduced product effectiveness.

    Product
    DYNAREX Dynarex SWABSTICK, PVP (3/PK 25/BX 10BX/CS) Catalog #1202
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1404-2022·2022-08-31

    Dr. Scholls Wart and Callus Remover Products Recalled for Storage Deviation

    Family Dollar Stores is recalling Dr. Scholls Clear Away Wart Remover, Callus Remover Pads, and Corn Removers distributed April 30 to June 10, 2022, due to improper storage conditions.

    Product
    DR SCHOLLS CLR AWAY LIQ WART REMVR 20CT SKU 998384 DR SCHOLLS CALLUS REMOVER PADS 4CT SKU 998431 DR SCHOLLS CORN REMOVERS 9CT SKU 998403 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1413-2022·2022-08-31

    Vaseline Eczema Calming Therapy Cream Recalled for Storage Temperature Violations

    Family Dollar Stores is recalling Vaseline Eczema Calming Therapy Cream (6.8 oz) distributed nationwide from April 30 to June 10, 2022, because the product was held outside appropriate storage temperature conditions in violation of CGMP requirements.

    Product
    VASELINE ECZEMA CALMING THERPY CRM 6.8 OZ 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 (Devices)·Z-1576-2022·2022-08-31

    Baxter Syringe Tip Caps Recalled Due to Sterile Packaging Barrier Failure

    Baxter Healthcare is recalling DISCPAC Syringe Tip Caps due to potential packaging defects that may not maintain sterile barriers. The recall affects approximately 63,190 units distributed worldwide.

    Product
    Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Orange: a) 25 pack, REF H93867025, b) 100 pack, REF H93867100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1448-2022·2022-08-31

    Bismuth-Based Antacids Recalled Due to Improper Storage Conditions

    Multiple bismuth-based antacid products distributed by Family Dollar Stores are being recalled due to storage temperature deviations that violate manufacturing standards. No illnesses have been reported.

    Product
    GUARDIAN BISMUTH CHWBLE CHRY TABS 30 CTSKU 902321 RIC BISMUTH MAXIMUM STRENGTH 8 FL OZ SKU 914325 PEPTO BISMOL ORIGINAL 8 FL OZ SKU 914324 RIC BISMUTH REG STRENGTH CHERRY 8 FL OZ SKU 914781 PEPTO BISMOL CHERRY 8 FL OZ SKU 916063 PEPTO B LIQUID ORIGINAL TRAVEL 3.4 FL O
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1369-2022·2022-08-31

    Hydrogen Peroxide Recalled Due to Improper Storage Conditions

    Family Dollar Stores is recalling Hydrogen Peroxide 16 oz. and 32 oz. bottles distributed from April 30 to June 10, 2022 due to storage outside required temperature ranges. Products have SKUs 909221 and 901675.

    Product
    Hydrogen Peroxide 16 fl. oz. and 32 oz. bottles 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 (Drugs)·D-1382-2022·2022-08-31

    Orajel Non Med Teething Gel Recalled for Improper Storage Conditions

    Orajel Non Med Teething Gel 0.125 oz is being recalled by Family Dollar Stores due to products being held outside appropriate storage temperature conditions. No illnesses have been reported.

    Product
    ORAJEL NON MED TEETHING GEL 0.125 OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    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-1395-2022·2022-08-31

    QP Motion Sickness Tablet 8 CT Recalled for Improper Storage Conditions

    Family Dollar Stores is recalling QP Motion Sickness Tablet 8 CT (SKU 901583) packages distributed nationwide from April 30 to June 10, 2022, due to improper storage temperature conditions.

    Product
    QP MOTION SICKNESS TABLET 8 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 (Devices)·Z-1614-2022·2022-08-31

    McKesson and Metrex Research Glutaraldehyde Disinfectants Recalled Due to Temperature Excursion

    McKesson and Metrex Research are recalling glutaraldehyde disinfectants due to facility temperature excursions from June to August 2021 that may have reduced product effectiveness. Affected lots were distributed nationwide between June 1 and September 30, 2021.

    Product
    a. McKesson DISINFECTANT, GLUTARALDEHYDE 28DAY (4GL/CS) MGM68, Model Number: 68-102800. b. METREX RESEARCH McKesson 14-Day Glutaraldehyde Solution DISINFECTANT, GLUTARALDEHYDE 14DAY (4GL/CS) MGM68 Model Number: 68-101400. c. METREX RESEARCH McKesson SOLUTION, GLUT 2.5%
    Category
    Medical Device
    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 (Devices)·Z-1574-2022·2022-08-31

    Vanta Clinician Programmer Software Cannot Connect with Multiple Implants

    The Vanta Clinician Programmer Application may fail to connect with Vanta neurostimulators when a patient has multiple devices implanted. This prevents programming of pain therapy settings in patients with multiple implants.

    Product
    Vanta Clinician Programmer Application, Model A71200. For programming of the Medtronic Model 977006 Vanta implantable neurostimulators for pain therapy.
    Category
    Medical Device
    Distribution
    50 states
  • 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-1370-2022·2022-08-31

    Deodorant and Antiperspirant Products Recalled for Temperature Storage Deviations

    Family Dollar Stores is recalling multiple deodorant and antiperspirant products because they were stored outside appropriate temperature conditions. No illnesses or injuries have been reported.

    Product
    SUAVE INV SLD PWDR 1.2 OZ SKU2004504 SUAVE AP INV SOLID SWEET PEA 1.2 OZ SKU 2004622 LADY SPEED STICK AP WILD FREESSIA 1.4OZ SKU 2005184 SUAVE AP DEOD POWDER 2.6 OZ 2PK SKU 2028126 SCRT IN SLD PWDR FRSH 2.1OZ 2PK SKU 2028363 LADY SPD STK AP INV PWDR 1.4OZ SKU 2028365
    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-1449-2022·2022-08-31

    Family Dollar Anti-Diarrheal Products Recalled for Improper Storage Conditions

    Family Dollar Stores has recalled specific loperamide anti-diarrheal products distributed between April 30 and June 10, 2022, due to improper storage temperature conditions. Consumers should discontinue use and return affected products.

    Product
    GS ANTI DIARRHEAL LOPERAMIDE CAPLET 12 CT SKU 915632 IMODIUM AD MINT 4 OZ SKU 902080 IMODIUM AD CAPLET 6 CT SKU 915628 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1578-2022·2022-08-31

    PICS Ground Cinnamon Recalled Due to Mislabeling as Cumin

    PICS Ground Cinnamon distributed to Price Chopper stores in Massachusetts is being recalled because the product actually contains cumin but is mislabeled as cinnamon.

    Product
    PICS Ground Cinnamon NET WT 16 OZ (453g) UPC 4173505270
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-1463-2022·2022-08-31

    Maxim Instant Foam Hand Sanitizer recalled due to expired active ingredient

    Midlab Incorporated is recalling Maxim Instant Foam Hand Sanitizer nationwide. The product was manufactured using expired benzalkonium chloride, potentially compromising effectiveness.

    Product
    Maxim Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%) packaged in a) 1 U.S. Gallon (3.78 Liters) drums UPC 7 61841 02502 6 and b) 55 U.S. Gallon drums (208 Liters) UPC 0 07 61841 02504 0, Midlab 140 Private Brand Way, Athens, TN 37303
    Category
    Drug
    Distribution
    0 states
  • 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 (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-1600-2022·2022-08-31

    Temno Soft Tissue Biopsy Device Recalled for Temperature Exposure

    Merit Medical Systems Temno soft tissue biopsy devices may have lost effectiveness due to storage temperature excursions between June and August 2021. The recall affects all lots received between June 1 and September 30, 2021.

    Product
    MERIT MEDICAL SYSTEMS Temno Soft Tissue Biopsy Device Temno 14 Gauge 6 cm Length Beveled Sharp Tip Model Number: T146
    Category
    Medical Device
    Distribution
    Distributed nationwide