The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Filters

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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

10501–10525 of 18028

  • SevereFDA (Drugs)·D-1093-2017·2017-08-23

    Lupin Recalls Mibelas 24 Fe Contraceptive Tablets Due to Sequence Error

    Lupin Limited is recalling Mibelas 24 Fe tablets because the first four pills in the packet are brown instead of the last four, and the expiry/lot was not printed on the package.

    Product
    Mibelas 24 Fe (Norethindrone acetate and Ethinyl estradiol 1 mg/0.02 mg chewable and ferrous Fumarate 75 mg) Tablets, wallet of 28 tablets (NDC 68180-911-11), Carton of 3 wallets (NDC 68180-911-13), Rx Only, Manufactured by: Lupin Limited, India, Distributed by Lupin Pharmaceutic
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1085-2017·2017-08-23

    Hardcore Formulations Recalls D-ZINE Rapid Size and Strength Capsules

    Hardcore Formulations is recalling D-ZINE Rapid Size and Strength capsules because they contain unapproved active ingredients.

    Product
    D-ZINE Rapid Size and Strength capsules, 10mgs, 90 count bottle, Hardcore Formulations, UPC: 7 48252 86193 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1084-2017·2017-08-23

    FDA Recalls Ultra-Sten Capsules Marketed Without Approval

    Hardcore Formulations is recalling Ultra-Sten capsules because they contain unapproved ingredients and were marketed without an approved NDA or ANDA.

    Product
    ULTRA-STEN Rapid Size and Strength capsules, 10 mgs, 90 count bottle, Hardcore Formulations UPC: 7 48252 68763 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1096-2017·2017-08-23

    FDA Recalls Unapproved Caffeine Powder Marketed Without NDA Approval

    Global Marketing Enterprises is recalling 52.5 kg of unapproved caffeine powder marketed with stimulant claims and lacking adequate directions for use.

    Product
    Caffeine Powder, Anhydrous, Pharmaceutical Grade, 100% Pure caffeine, 250 g (8.8 oz)., 1250 servings, Packed By: LifeLine Nutrients Corp, 1801 S. Canal St, Chicago, IL 60616, UPC 021754905076
    Category
    Drug
    Distribution
    3 states
  • SevereFDA (Drugs)·D-1091-2017·2017-08-23

    ICU Medical Recalls 0.9% Sodium Chloride Injection Due to Particulate Matter

    ICU Medical Inc. is recalling 436,716 units of 0.9% Sodium Chloride Injection due to the presence of stainless steel particulate matter.

    Product
    0.9% Sodium Chloride Injection, USP in 1000 mL Single Dose Flexible Container, Hospira, Inc., Lake Forest, IL 60045 USA --- NDC# 0409-7983-09
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1094-2017·2017-08-23

    AvKARE Recalls Voriconazole Tablets Due to Impurity Specification Failure

    AvKARE Inc. is recalling specific lots of Voriconazole Tablets, 200 mg, because they failed impurity specifications for a related compound.

    Product
    Voriconazole Tablets, 200 mg, 20-count cartons (4 x 5) Unit Dose, Rx only, Manufactured for: AvKARE, Inc. Pulaski, TN 38478, NDC 50268-804-12
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1088-2017·2017-08-23

    Akorn Recalls Chlorhexidine Gluconate Oral Rinse Due to Crystallization

    Akorn Inc is recalling Chlorhexidine Gluconate Oral Rinse unit dose cups because crystallization caused subpotent assay results.

    Product
    Chlorhexidine Gluconate Oral Rinse, 0.12%, 15 mL Unit Dose Cup, a) unit dose cup (NDC 50383-720-15), b) 100-count tray (NDC 50383-720-19), Rx Only, Hi-Tech Pharmacal Co. Inc., Amityville, NY 11701.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1108-2017·2017-08-23

    Linde Eckstein Recalls SPF 10 Liquid Make-Up Due to Subpotent Drug

    Linde Eckstein is recalling specific lots of Make Up Perfect sand SPF 10 liquid make-up because the SPF 10 protection claim cannot be fully guaranteed.

    Product
    Make Up Perfect sand (Titanium Dioxide) SPF 10 liquid make-up, 1 oz. Net Wt. 30 ml bottle, Art. 03320, Made in Germany, Doctor Eckstein, Linde Eckstein GMBH Co. Kg, 90522 Oberasbach, Germany, UPC 4 035219 033200.
    Category
    Drug
    Distribution
    0 states
  • LowFDA (Drugs)·D-1106-2017·2017-08-23

    Linde Eckstein Recalls Make Up Perfect Ivory SPF 10 Liquid Make-Up

    Linde Eckstein is recalling Make Up Perfect Ivory SPF 10 liquid make-up because the SPF 10 protection claim cannot be guaranteed.

    Product
    Make Up Perfect ivory (Titanium Dioxide) SPF 10 liquid make-up, 1 oz. Net Wt. 30 ml bottle, Art. 03300, Made in Germany, Doctor Eckstein, Linde Eckstein GMBH Co. Kg, 90522 Oberasbach, Germany, UPC 4 035219 033002.
    Category
    Drug
    Distribution
    0 states
  • LowFDA (Drugs)·D-1089-2017·2017-08-23

    Akorn Recalls Halyard Chlorhexidine Oral Rinse Due to Crystallization

    Akorn Inc is recalling Halyard 24-Hour Oral Care Kits containing chlorhexidine gluconate oral rinse due to crystallization and subpotent assay results.

    Product
    Halyard 24-Hour Oral Care Kit q2, contains 2x15 mL Unit Dose Cups 0.12% Chlorhexidine Gluconate Oral Rinse. Manufactured by Halyard Health Inc., 5405 Windward Parkway, Alpharetta, GA 30004. Distributed by Halyard Sales, LLC Alpharetta, GA 30004. REF # 97012
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1109-2017·2017-08-23

    Linde Eckstein Recalls Make Up Perfect SPF 10 Liquid Make-up

    Linde Eckstein Gmbh + Co KG is recalling Make Up Perfect dark tan SPF 10 liquid make-up because the SPF 10 protection claim cannot be guaranteed.

    Product
    Make Up Perfect dark tan (Titanium Dioxide) SPF 10 liquid make-up, 1 oz. Net Wt. 30 ml bottle, Art. 03340, Made in Germany, Doctor Eckstein, Linde Eckstein GMBH Co. Kg, 90522 Oberasbach, Germany, UPC 4 035219 033408.
    Category
    Drug
    Distribution
    0 states
  • LowFDA (Drugs)·D-1102-2017·2017-08-23

    Linde Eckstein SPF 10 Liquid Make-up Recalled for Subpotent Drug Claim

    Linde Eckstein is recalling specific lots of SPF 10 liquid make-up because the sun protection factor claim cannot be fully guaranteed.

    Product
    Make Up Transparent sand (Titanium Dioxide) SPF 10 liquid make-up, 1 oz. Net Wt. 30 ml bottle, Art. 03220, Made in Germany, Doctor Eckstein, Linde Eckstein GMBH Co. Kg, 90522 Oberasbach, Germany, UPC 4 035219 032203.
    Category
    Drug
    Distribution
    0 states
  • LowFDA (Drugs)·D-1100-2017·2017-08-23

    Linde Eckstein SPF 10 Liquid Make-up Recalled for Subpotent Claims

    Linde Eckstein is recalling 373 bottles of SPF 10 liquid make-up because the sun protection claim cannot be guaranteed.

    Product
    Make Up Transparent ivory (Titanium Dioxide) SPF 10 liquid make-up, 1 oz. Net Wt. 30 ml bottle, Art. 03200, Made in Germany, Doctor Eckstein, Linde Eckstein GMBH Co. Kg, 90522 Oberasbach, Germany, UPC 4 035219 032005.
    Category
    Drug
    Distribution
    0 states
  • LowFDA (Drugs)·D-1110-2017·2017-08-23

    Linde Eckstein Recalls SPF 10 Liquid Make-Up Due to Subpotent Labeling

    Linde Eckstein is recalling Make Up Perfect terra SPF 10 liquid make-up because the sun protection factor claim cannot be fully guaranteed.

    Product
    Make Up Perfect terra (Titanium Dioxide) SPF 10 liquid make-up, 1 oz. Net Wt. 30 ml bottle, Art. 03350, Made in Germany, Doctor Eckstein, Linde Eckstein GMBH Co. Kg, 90522 Oberasbach, Germany, UPC 4 035219 033507.
    Category
    Drug
    Distribution
    0 states
  • LowFDA (Drugs)·D-1107-2017·2017-08-23

    Linde Eckstein SPF 10 Liquid Make-up Recalled for Subpotent Sun Protection

    Linde Eckstein is recalling SPF 10 liquid make-up because the sun protection claim cannot be fully guaranteed. Consumers should stop using the product.

    Product
    Make Up Perfect pastel (Titanium Dioxide) SPF 10 liquid make-up, 1 oz. Net Wt. 30 ml bottle, Art. 03310, Made in Germany, Doctor Eckstein, Linde Eckstein GMBH Co. Kg, 90522 Oberasbach, Germany, UPC 4 035219 033101.
    Category
    Drug
    Distribution
    0 states
  • LowFDA (Drugs)·D-1083-2017·2017-08-23

    KVK-Tech Recalls Phentermine Hydrochloride Capsules Due to Impurity Failures

    KVK-Tech, Inc. is recalling specific lots of Phentermine Hydrochloride capsules because they failed impurity specifications during stability testing.

    Product
    PHENTERMINE HYDROCHLORIDE — PHENTERMINE HYDROCHLORIDE (PHENTERMINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1101-2017·2017-08-23

    Linde Eckstein SPF 10 Liquid Make-up Recalled for Subpotent Drug Claim

    Linde Eckstein is recalling SPF 10 liquid make-up because the sun protection claim cannot be fully guaranteed. The product was distributed throughout the United States.

    Product
    Make Up Transparent pastel (Titanium Dioxide) SPF 10 liquid make-up, 1 oz. Net Wt. 30 ml bottle, Art. 03210, Made in Germany, Doctor Eckstein, Linde Eckstein GMBH Co. Kg, 90522 Oberasbach, Germany, UPC 4 035219 032104.
    Category
    Drug
    Distribution
    0 states
  • LowFDA (Drugs)·D-1104-2017·2017-08-23

    Linde Eckstein SPF 10 Liquid Make-up Recalled for Subpotent Drug Concerns

    Linde Eckstein is recalling specific lots of SPF 10 liquid make-up because the sun protection claim cannot be fully guaranteed.

    Product
    Make Up Transparent dark tan (Titanium Dioxide) SPF 10 liquid make-up, 1 oz. Net Wt. 30 ml bottle, Art. 03240, Made in Germany, Doctor Eckstein, Linde Eckstein GMBH Co. Kg, 90522 Oberasbach, Germany, UPC 4 035219 032401.
    Category
    Drug
    Distribution
    0 states
  • LowFDA (Drugs)·D-1105-2017·2017-08-23

    Linde Eckstein SPF 10 Liquid Make-up Recalled for Subpotent Drug Claim

    Linde Eckstein Gmbh + Co KG is recalling SPF 10 liquid make-up because the sun protection claim cannot be fully guaranteed.

    Product
    Make Up Transparent terra (Titanium Dioxide) SPF 10 liquid make-up, 1 oz. Net Wt. 30 ml bottle, Art. 03250, Made in Germany, Doctor Eckstein, Linde Eckstein GMBH Co. Kg, 90522 Oberasbach, Germany, UPC 4 035219 032500.
    Category
    Drug
    Distribution
    0 states
  • LowFDA (Drugs)·D-1097-2017·2017-08-23

    Linde Eckstein Recalls Beautipharm Moisturizing Balm Due to SPF Labeling Concerns

    Linde Eckstein is recalling 478 bottles of Beautipharm All Day Moisturizing Balm SPF 10 because the SPF 10 protection claim cannot be fully guaranteed.

    Product
    Beautipharm All Day Moisturizing Balm SPF 10 (Octocrylene 4% and Octyl methoxycinnamide 4%) Facial Cream, 1.66 oz. Net. Wt. 50 ml bottle, Art. 03120 Made in Germany, Doctor Eckstein, Linde Eckstein GMBH Co. Kg, 90522 Oberasbach, Germany. UPC 4 035219 032005.
    Category
    Drug
    Distribution
    0 states
  • LowFDA (Drugs)·D-1103-2017·2017-08-23

    Linde Eckstein Recalls Make Up Perfect Caramel SPF 10 Liquid Make-Up

    Linde Eckstein Gmbh + Co KG is recalling Make Up Perfect Caramel SPF 10 liquid make-up because the SPF 10 protection claim cannot be fully guaranteed.

    Product
    Make Up Perfect caramel (Titanium Dioxide) SPF 10 liquid make-up, 1 oz. Net Wt. 30 ml bottle, Art. 03330, Made in Germany, Doctor Eckstein, Linde Eckstein GMBH Co. Kg, 90522 Oberasbach, Germany, UPC 4 035219 032302.
    Category
    Drug
    Distribution
    0 states
  • LowFDA (Drugs)·D-1098-2017·2017-08-23

    Linde Eckstein Recalls Beautipharm Body Moisturizing Balm Due to Subpotent SPF

    Linde Eckstein is recalling Beautipharm Body Moisturizing Balm SPF 10 because the sun protection factor claim cannot be fully guaranteed.

    Product
    Beautipharm Body Moisturizing Balm SPF 10 (Octocrylene 4% and Octyl methoxycinnamide 4%) Body Lotion, 8.3 oz. Net. Wt. 250 ml bottle, Art. 03150 Made in Germany, Doctor Eckstein, Linde Eckstein GMBH Co. Kg, 90522 Oberasbach, Germany. UPC 4 035219 031503.
    Category
    Drug
    Distribution
    0 states
  • LowFDA (Drugs)·D-1090-2017·2017-08-23

    Akorn Recalls Halyard Chlorhexidine Oral Rinse Due to Crystallization

    Akorn Inc is recalling Halyard 24-Hour Oral Care Kits containing chlorhexidine gluconate oral rinse due to crystallization and subpotent assay results.

    Product
    Halyard 24-Hour Oral Care Kit q4, contains 2x15 mL Unit Dose Cups 0.12% Chlorhexidine Gluconate Oral Rinse. Manufactured by Halyard Health Inc., 5405 Windward Parkway, Alpharetta, GA 30004. Distributed by Halyard Sales, LLC Alpharetta, GA 30004. REF # 97014
    Category
    Drug
    Distribution
    Distributed nationwide