Colorado recalls
3887 federal recalls on file affecting Colorado - 512 Colorado-specific plus 3375 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-04-15FDA-DeviceSiemensClass IINationwideContact Siemens about your ARTIS imaging system
During patient examinations, the system may sporadically display a major increase of the x-ray dose applied to the patient. Despite the reported dose showing significantly higher, the actual applied x-ray dose levels are in accordance with the system settings and imaging conditions, as well as the applicable regulatory requirements.
- 2026-04-15FDA-DrugTevaClass IINationwideStop using recalled Teva Clonidine patches
CGMP Deviations: use of an unapproved raw material
- 2026-04-15FDA-DrugTevaClass IINationwideCheck your Clonidine patch lot numbers
CGMP Deviations: use of an unapproved raw material
- 2026-04-15FDA-DrugTevaClass IINationwideStop using recalled Teva Clonidine patches
CGMP Deviations: use of an unapproved raw material
- 2026-04-15FDA-DrugGE HealthcareClass IINationwideCheck Omnipaque injection lot numbers immediately
Presence of particulate matter
- 2026-04-15FDA-DrugGE HealthcareClass IINationwideCheck GE Healthcare Omnipaque injection lot numbers
Presence of particulate matter
- 2026-04-15FDA-DrugViatris, Inc.Class IINationwideCheck your Xanax XR 3 mg prescription bottle
Failed Dissolution Specifications
- 2026-04-15FDA-DrugPreferred Pharmaceuticals, Inc.Class IINationwideStop using Preferred Pharmaceuticals Artificial Tears
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFagron Compounding ServicesClass IINationwideStop using Fagron Vancomycin HCL IV bags
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
- 2026-04-15FDA-DrugFagron Compounding ServicesClass IINationwideVancomycin HCI, 1.5 grams added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5085-01
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
- 2026-04-15FDA-DrugFagronClass IINationwideVancomycin HCI, 1.25 grams added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5083-01
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
- 2026-04-15FDA-DrugFagron Compounding ServicesClass IINationwideStop using Fagron norepinephrine injection
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
- 2026-04-15FDA-DrugFagron Compounding ServicesClass IINationwideDo not use Fagron norepinephrine injection
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
- 2026-04-15FDA-DrugFresenius KabiClass IINationwideStop using Fresenius Kabi dextrose injection
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFresenius KabiClass IINationwideDo not use Fresenius Kabi dextrose injection
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFresenius KabiClass IINationwideStop using Fresenius Kabi dextrose injection
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFresenius KabiClass IINationwideStop using Fresenius Kabi sodium chloride injection
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFresenius KabiClass IINationwideStop using Fresenius Kabi saline injection
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFresenius KabiClass IINationwideStop using Fresenius Kabi saline injection
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFresenius KabiClass IINationwide0.9% Sodium Chloride Injection, USP, 900 mg per 100 mL (9 mg per mL) 250 mL in a Single Dose freeflex bag, Rx only, BD Becton, Dickson and Company, 1 Beckton Drive, Franklin Lakes, NJ 07417, Distributed by BD, Manufactured by: Fresenius Kabi USA, LLC ("Fresenius Kabi"), Unit of Sale NDC Number: 17271-701-05.
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFresenius KabiClass IINationwideDo not use Fresenius Kabi saline injection
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFresenius KabiClass IINationwideStop using Fresenius Kabi saline injection
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFresenius KabiClass IINationwideStop using Fresenius Kabi sodium chloride injection
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFresenius KabiClass IINationwideStop using Fresenius Kabi saline injection
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFresenius KabiClass IINationwideStop using Fresenius Kabi saline injection
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFresenius KabiClass IINationwideStop using Fresenius Kabi saline injection
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFresenius KabiClass IINationwideStop using Fresenius Kabi saline injection
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugCiplaClass IINationwideStop using Cipla Lanreotide Injection
Lack of Assurance of Sterility: Due to an FDA observation at the contract manufacturing site for deficiencies in their visual inspection procedure.
- 2026-04-15FDA-DrugCiplaClass IINationwideDo not use Cipla Lanreotide Injection
Lack of Assurance of Sterility: Due to an FDA observation at the contract manufacturing site for deficiencies in their visual inspection procedure.
- 2026-04-09FDA-PRNationwideStop using Morovan nail polish remover
Nail Polish Remover recalled due to the detection of methylene chloride and chloroform in the affected product—both hazardous substances that are strictly prohibited in cosmetic formulations.
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