The Recall Desk

Hazard

Cosmetic Defect recalls

59 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
59
Critical
0
Severe
0
Most recent
2026-03-11

Of the 59 cosmetic defect recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all cosmetic defect recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

51–59 of 59

  • LowFDA (Drugs)·D-1057-2016·2016-07-06

    KVK-Tech Recalls Benzphetamine Hydrochloride Tablets Due to Cosmetic Scuffing

    KVK-Tech, Inc. is recalling specific lots of Benzphetamine Hydrochloride Tablets due to cosmetic scuffing marks on the tablets.

    Product
    Benzphetamine Hydrochloride Tablets, 50 mg, 30-count bottle, RX only, Mfd by: KVK-TECH, INC., Newtown, PA 18940, NDC 10702-0040-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1409-2015·2015-04-22

    Biomet 3i Recalls T3 Dental Implants Due to Machine Fluid Discoloration

    Biomet 3i, LLC is recalling 620 T3 Non-Platform Switched Tapered Dental Implants because contact with residual machine fluid caused discoloration.

    Product
    3i T3 Non-Platform Switched Tapered Implant Rx Only; 3.25 x 8.5 - 15.0 mm Dental Implants.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0804-2015·2014-12-24

    AGFA Healthcare Recalls Radiomat M+ NIF Films Due to Coating Artifacts

    AGFA Healthcare is recalling 142 units of Radiomat M+ NIF films because the coating may show small bright thin lines when processed.

    Product
    Radiomat M+ NIF 14 x 17, Radiomat M+ NIF 35CM x 43CM, Radiomat M+ NIF 10 x 12, Radiomat M+ NIF 25,4CM x 30,5CM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0080-2015·2014-11-05

    Keystone Laboratories Recalls Long Aid Curl Activator Gel Due to Cloudy Appearance

    Keystone Laboratories is recalling Long Aid Curl Activator Gel because the product has a cloudy appearance. The recall covers 39,498 units distributed to several US states and the Bahamas.

    Product
    LONG AID Curl Activator Gel, NET WT. 16.4 OZ. (464.9g), KEYSTONE LABORATORIES, 1103 KANSAS STREET, MEMPHIS, TN 38106, UPC 070596003655
    Category
    Consumer Product
    Distribution
    10 states
  • LowFDA (Drugs)·D-839-2013·2013-08-14

    West-Ward Recalls Ethambutol Hydrochloride Tablets Due to Surface Ink Defects

    West-Ward Pharmaceutical Corp. is recalling 118 bottles of Ethambutol Hydrochloride Tablets 400 mg due to out-of-specification surface ink defects.

    Product
    VersaPharm Incorporated, Ethambutol Hydrochloride Tablets, USP 400 mg 60 tablets, Rx Only, Mfd. for VersaPharm Incorporated Marietta, GA 30065-1509; Mfd. by: West-ward Pharmaceuticals Corp., Eatontown, NJ 07724 NDC 61748-014-06,
    Category
    Drug
    Distribution
    1 state
  • LowFDA (Drugs)·D-246-2013·2013-04-17

    Teva Recalls Jolessa Tablets Due to Appearance Specification Failures

    Teva Pharmaceuticals is recalling specific lots of Jolessa tablets because they failed appearance specifications. The recall is nationwide.

    Product
    JOLESSA — JOLESSA (LEVONORGESTREL / ETHINYL ESTRADIOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-245-2013·2013-04-17

    Teva Recalls Portia Tablets Due to Appearance Specification Failures

    Teva Pharmaceuticals is recalling Portia (levonorgestrel and ethinyl estradiol) tablets because they failed appearance specifications.

    Product
    PORTIA — PORTIA (LEVONORGESTREL AND ETHINYL ESTRADIOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-189-2013·2013-03-13

    VersaPharm Ethambutol Tablets Recalled for Discoloration

    West-ward Pharmaceutical Corp. is recalling VersaPharm Ethambutol Tablets USP 400 mg because the tablet cores may be discolored.

    Product
    VERSAPHARM Ethambutol Tablets, USP,400 mg, Rx Only a)60 tablets, NDC 61748-014-06, b)90 tablets, NDC 61748-014-09, c)100 tablets, NDC 61748-014-01, d)1000 tablets, NDC 61748-014-10, e) blister pack (10s) 61748-014-11 Manufactured for: VersaPharm Incorporated Marietta, GA
    Category
    Drug
    Distribution
    1 state