State

Colorado product recalls

72,919 recalls have nationwide distribution and so reach Colorado. 6,941 additional recalls listed Colorado specifically in their distribution scope.

What the numbers show

Total: 6,941
Critical: 1,218
Severe: 1,507
Most recent: 2026-09-09

Of the 6,941 recalls naming Colorado we have scored against our rubric, 1,218 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,507 (22%) are Severe.

Which agencies issued them

These figures cover only the 6,941 recalls whose distribution notice names Colorado specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2351–2375 of 79860

HighFDA (Devices)·Z-1821-2026·2026-04-22
Elegance anterior cervical plates recalled over burrs on finished product
Elegance Anterior Cervical Plates are being recalled over a quality issue involving the presence of burrs on the finished plate. The action covers 511 units.
Product
Brand Name: Elegance¿ Anterior Cervical Plate Product Name: ELEGANCE 1 LEVEL CERVICAL PLATE, ELEGANCE 2 LEVEL CERVICAL PLATE, ELEGANCE 3 LEVEL CERVICAL PLATE, ELEGANCE 4 LEVEL CERVICAL PLATE Model/Catalog Number: See Excel sheet attached named "FDA 5072 Product Information" So
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1811-2026·2026-04-22
Arjo Tenor patient lift actuators may lose the ability to hold load
Arjo Tenor mobile passive patient lifts are being recalled because an internal actuator component in one production batch may not meet the required mechanical strength.
Product
Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0449-2026·2026-04-22
Cipla cinacalcet 30 mg tablets exceed the nitrosamine daily intake limit
Cipla is recalling Cinacalcet Hydrochloride Tablets, 30 mg, over CGMP deviations and the presence of N-Nitroso Cinacalcet above the acceptable daily intake limit. 113,336 bottles are affected.
Product
CINACALCET — CINACALCET (CINACALCET)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1824-2026·2026-04-22
Centurion circumcision kits distributed without the required sterilization process
Medline is recalling one lot of Centurion Circumcision Kits that was distributed without undergoing the required sterilization process and is therefore not sterile. 640 kits are affected.
Product
CENTURION Circumcision Kit, Medline Kit Number/SKU CIT7050F
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0487-2026·2026-04-22
Skin Script blemish spot treatment recalled for failing stability specifications
Skin Script Blemish Spot Treatment containing 1% salicylic acid is being recalled after it failed stability specifications. The action covers 28,163 bottles.
Product
Blemish Spot Treatment (Salicylic Acid) 1%, .5 fl oz (15 ml) bottles, Skin Script, Chandler, AZ 85226, UPC 6 10563 13873 9.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0450-2026·2026-04-22
Cipla cinacalcet 60 mg tablets exceed the nitrosamine daily intake limit
Cipla is recalling Cinacalcet Hydrochloride Tablets, 60 mg, over CGMP deviations and the presence of N-Nitroso Cinacalcet above the acceptable daily intake limit. 96,096 bottles are affected.
Product
CINACALCET — CINACALCET (CINACALCET)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1823-2026·2026-04-22
Gentuity HF-OCT imaging systems may repeat frames during catheter pullback
Gentuity is issuing a correction for HF-OCT Imaging Systems because frames may repeat during pullback with Vis-Rx catheters, affecting longitudinal length measurements.
Product
Gentuity HF-OCT Imaging System Model G10-01; Software version 23.2.13;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0451-2026·2026-04-22
Cipla cinacalcet 90 mg tablets exceed the nitrosamine daily intake limit
Cipla is recalling Cinacalcet Hydrochloride Tablets, 90 mg, over CGMP deviations and the presence of N-Nitroso Cinacalcet above the acceptable daily intake limit. 63,192 bottles are affected.
Product
CINACALCET — CINACALCET (CINACALCET)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0510-2026·2026-04-22
Apotek desmopressin nasal spray recalled over dislodged or missing cap liners
Apotek is recalling one lot of Desmopressin Nasal Spray, USP because of a defect in a batch of bottle caps involving dislodged or missing cap liners.
Product
DESMOPRESSIN ACETATE — DESMOPRESSIN ACETATE (DESMOPRESSIN ACETATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0476-2026·2026-04-22
Taro fluocinonide cream 30 g tubes fail viscosity stability specifications
Taro is recalling one lot of Fluocinonide 0.05% Cream in 30 g tubes after stability testing returned viscosity results above the specification limit. 41,712 tubes are affected.
Product
FLUOCINONIDE — FLUOCINONIDE (FLUOCINONIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0461-2026·2026-04-22
MGC Health sugar free honey lemon cough drops recalled after inspection
MGC Health sugar free Menthol Cough Suppressant Oral Anesthetic Cough Drops, honey lemon, 25-count bags, are being recalled following FDA observations at the manufacturing facility.
Product
MGC HEALTH — MGC HEALTH (COUGH DROPS HONEY SUGAR-FREE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0477-2026·2026-04-22
Taro fluocinonide cream 60 g tubes fail viscosity stability specifications
Taro is recalling one lot of Fluocinonide 0.05% Cream in 60 g tubes after stability testing returned viscosity results above the specification limit. 2,640 tubes are affected.
Product
FLUOCINONIDE — FLUOCINONIDE (FLUOCINONIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0458-2026·2026-04-22
Caring Mill cherry cough drops recalled after facility inspection findings
Caring Mill Menthol Cough Suppressant Oral Anesthetic Cough Drops, cherry, 90-count bags, are being recalled following FDA observations at the manufacturing facility.
Product
CARING MILL COUGH DROPS CHERRY — CARING MILL COUGH DROPS CHERRY (MENTHOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0462-2026·2026-04-22
MGC Health 30-count honey lemon cough drops recalled after inspection findings
MGC Health Menthol Cough Suppressant Oral Anesthetic Cough Drops, honey lemon, 30-count bags, are being recalled following FDA observations at the manufacturing facility.
Product
MGC HEALTH — MGC HEALTH (COUGH DROPS HONEY)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0465-2026·2026-04-22
Quality Choice cherry cough drops recalled after facility inspection findings
QC Quality Choice Menthol Cough Suppressant Oral Anesthetic Cough Drops, cherry flavour, 30-count bags, are being recalled following FDA observations at the manufacturing facility.
Product
QUALITY CHOICE — QUALITY CHOICE (COUGH DROPS HONEY LEMON SUGAR FREE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0463-2026·2026-04-22
MGC Health 80-count honey lemon cough drops recalled after inspection findings
MGC Health Menthol Cough Suppressant Oral Anesthetic Cough Drops, honey lemon, 80-count bags, are being recalled following FDA observations at the manufacturing facility.
Product
MGC HEALTH — MGC HEALTH (COUGH DROPS HONEY)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0479-2026·2026-04-22
Nephron albuterol inhalation solution vials recalled over an illegible label
Nephron is recalling one lot of Albuterol Sulfate Inhalation Solution 0.5% unit-dose vials because of an illegible label. The action covers 146,280 vials.
Product
Albuterol Sulfate Inhalation Solution, 0.5%, 25 mg/5 mL (5 mg/mL*), 30x5 mL Sterile Unit-Dose Vials, Rx only, nephron 503B Outsourcing facility, 4600 12th Street Extension, West Columbia, SC 29172, NDC 69374-330-05.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0468-2026·2026-04-22
Quality Choice honey lemon cough drops recalled after facility inspection findings
QC Quality Choice Menthol Cough Suppressant Oral Anesthetic Cough Drops, honey lemon flavour, 30-count bags, are being recalled following FDA observations at the manufacturing facility.
Product
QUALITY CHOICE — QUALITY CHOICE (COUGH DROPS HONEY LEMON)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1810-2026·2026-04-22
LinkBio CORE Workstation may display an incorrect planning date
LinkBio is recalling the CORE Workstation, a component of the CORE Shoulder System, because it may display an incorrect planning date on the Start Case menu screen.
Product
LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0480-2026·2026-04-22
glo Skin Beauty Remedy Gel recalled as a subpotent hydrocortisone product
Remedy Gel, hydrocortisone 1%, distributed by glo Skin Beauty is being recalled because the product is subpotent. The action covers 1,060 bottles.
Product
Remedy Gel, hydrocortisone 1%, 30 mL/ 1 fl oz per bottle, Distributed By: glo Skin Beauty, Denver, CO 80216. NDC 66915-531-12; 66915-531-13
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0456-2026·2026-04-22
Exchange Select honey lemon cough drops recalled after facility inspection findings
Exchange Select Menthol Cough Suppressant Oral Anesthetic Cough Drops, honey lemon, 30-count bags, are being recalled following FDA observations at the manufacturing facility.
Product
HONEY LEMON FLAVOR COUGH DROP — HONEY LEMON FLAVOR COUGH DROP (HONEY LEMON FLAVOR COUGH DROP)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0481-2026·2026-04-22
Skin Rehab calming hydrocortisone balm recalled as a subpotent drug
Skin Rehab Calming Skin Gel Hydrocortisone Balm, hydrocortisone 1%, is being recalled because the product is subpotent. The action covers 2,895 bottles.
Product
Skin Rehab, Calming Skin Gel, Hydrocortisone Balm, hydrocortisone 1%, .53oz net wt. (15.3g) per bottle, Distributed By: A.C.E. Inc., DFW Intl. Airport, Texas 75261, www.RHONDAALLISON.COM. NDC 66915-531-04
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0469-2026·2026-04-22
Quality Choice menthol cough drops recalled after facility inspection findings
QC Quality Choice Menthol Cough Suppressant Oral Anesthetic Cough Drops, menthol flavour, 30-count bags, are being recalled following FDA observations at the manufacturing facility.
Product
QUALITY CHOICE — QUALITY CHOICE (COUGH DROPS MENTHOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0457-2026·2026-04-22
Menthol Flavor Cough Drops Recalled Due to Potential Product Quality Issues
Xiamen Kang Zhongyuan Biotechnology Co., Ltd. is recalling Menthol Flavor Cough Drops due to quality concerns identified during an FDA inspection.
Product
MENTHOL FLAVOR COUGH DROP — MENTHOL FLAVOR COUGH DROP (MENTHOL FLAVOR COUGH DROP)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0464-2026·2026-04-22
Quality Choice sugar free black cherry cough drops recalled after inspection findings
QC Quality Choice sugar free Menthol Cough Suppressant Oral Anesthetic Cough Drops, black cherry, 25-count bags, are being recalled following FDA observations at the manufacturing facility.
Product
QUALITY CHOICE — QUALITY CHOICE (COUGH DROPS HONEY LEMON SUGAR FREE)
Category
Drug
Distribution
Distributed nationwide