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Safety Reports: Recall

Updated: May 18, 2025 9:08 AM

Real Time Reports

Recall notice

AVKARE Eye Drops Recalled Over Sterility Issues, United States

9 months ago •source avkare.com • details

BRS Analytical Service, LLC. has initiated a voluntary recall of various ophthalmic products due to manufacturing deviations identified during an FDA audit. The potential health hazard to users is currently unknown, but the deviations may lead to products of unacceptable quality. The recall was initiated after the… See more

#drugs #recall #unitedstates

Recalls AVKARE Eye Drops Recalled Over Sterility Issues BRS Analytical Service, LLC. has initiated a volunta... photo #1

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Recall notice

Sacred Tattoo Ink recalled due to Pseudomonas Aeruginosa Contamination, USA

10 months ago •source fda.gov • details

The FDA is alerting consumers, tattoo artists, and retailers of the potential for serious injury from use of tattoo inks that are contaminated with bacteria, including Pseudomonas aeruginosa. The affected products were distributed across the US.

Tattoo inks contaminated with pathogenic microorganisms can cause infections and lead… See more

#recall #cosmetics #unitedstates

Recalls Sacred Tattoo Ink recalled due to Pseudomonas Aeruginosa Contamination The FDA is alerting consumers... photo #1

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Recall notice

Male Enhancement Dietary Supplements recalled due to Undeclared Ingredients, USA

10 months ago •source fda.gov • details

HEALTH FIXER is voluntarily recalling all lots of dietary supplements by the name of Male Ultra, Malextra, Electro Buzz, Ultra Armor and Male Ultra Pro- blister packs of 10 capsules per box/carton to the consumer level. Laboratory analysis has found the products to be tainted with chloropretadalafil,… See more

#vitamins #recall #unitedstates

Recalls Male Enhancement Dietary Supplements recalled due to Undeclared Ingredients HEALTH FIXER is voluntar... photo #1

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Recall notice

Dexased™ and Dexmedvet™ Hydrochloride Injection recalled due to Particulate Matter, USA

10 months ago •source fda.gov • details

CRONUS PHARMA LLC, on behalf of Cronus Pharma Specialties, Hyderabad, India is issuing a voluntary recall involving one batch comprising two distinct lots: Dexased™ (Aspen) and Dexmedvet™ (Cronus Pharma LLC). Both products contain Dexmedetomidine Hydrochloride Injection 0.5 mg/mL, which is a prescription product in the United States… See more

#recall #animalveterinary #unitedstates

Recalls Dexased™ and Dexmedvet™ Hydrochloride Injection recalled due to Particulate Matter CRONUS PHARMA LLC... photo #1

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Recall notice

Timed Release Melatonin recalled due to mislabelling, Canada

10 months ago •source recalls-rappels.canada.ca • details

Vita Health Products Inc. has issued a recall for its Life Brand Timed Release Melatonin 10mg due to incorrect dosing instructions on the label. The recall is national and affects several lot numbers. The issue was discovered during routine quality control checks. The incorrect dosing instructions could… See more

#recall #canada

Recalls Timed Release Melatonin recalled due to mislabelling Vita Health Products Inc. has issued a recall f... photo #1

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Recall notice

Tower Air Fryers recalled due to Risk of Fire, UK

10 months ago •source gov.uk • details

Tower Air Fryers are being recalled due to a risk of fire. The product may overheat and ignite during use. The recall was announced by the Office for Product Safety and Standards on April 8, 2025. The products were sold by various retailers, including Argos, B&M Bargains,… See more

#recall #unitedkingdom

Recalls Tower Air Fryers recalled due to Risk of Fire Tower Air Fryers are being recalled due to a risk of f... photo #1

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Recall notice

Ropivacaine Hydrochloride Injection recalled due to Inert Fiber, USA

10 months ago •source fda.gov • details

Amneal Pharmaceutical LLC is recalling two lots of Ropivacaine Hydrochloride Injection, USP, 500mg/100mL, Infusion bags to the hospital/user level as the products may contain an inert fiber identified as polypropylene fibers from the IV bag. The recalled product was distributed nationwide to wholesalers/distributors between the dates of… See more

#recall #unitedstates

Recalls Ropivacaine Hydrochloride Injection recalled due to Inert Fiber Amneal Pharmaceutical LLC is recalli... photo #1

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Recall notice

Bausch + Lomb Recalls enVista Intraocular Lenses Due to Safety Concern, USA

11 months ago •source fda.gov • details

Bausch + Lomb Corporation a leading global eye health company dedicated to helping people see better to live better, today announced a voluntary recall of intraocular lenses (IOLs) on its enVista platform. This action was taken after the company received reports of complications, the cause of which… See more

#recall #unitedstates

Recalls Bausch + Lomb Recalls enVista Intraocular Lenses Due to Safety Concern Bausch + Lomb Corporation a l... photo #1

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Recall notice

FDA Warns Against Inhalation of Nitrous Oxide Products Due to Health Risks, USA

11 months ago •source fda.gov • details

####Update June 4th, 2025:
The FDA has expanded its list of brand names linked to nitrous oxide products to now include ExoticWhip, FastGas, and NITROX. These nitrous oxide tanks, canisters, and chargers are often sold online or at locations such as vape shops, gas stations, and smoke… See more

#recall #unitedstates

Recalls FDA Warns Against Inhalation of Nitrous Oxide Products Due to Health Risks Update June 4th, 2025:
Th... photo #1

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Recall notice

CAPS Phenylephrine 40 mg recalled due to visible black particulate matter, USA

1 year ago •source fda.gov • details

Central Admixture Pharmacy is recalling three lots of Phenylephrine 40 mg added to 0.9% Sodium Chloride 250 mL in 250 mL Excel Bags (NDC: 71285-6092-1) to the hospital level. The product is being recalled because CAPS was notified by their raw material supplier of the detection of… See more

#recall #drugs #unitedstates

Recalls CAPS Phenylephrine 40 mg recalled due to visible black particulate matter Central Admixture Pharmacy... photo #1

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Safety Reports: Recall

Real Time Reports

AVKARE Eye Drops Recalled Over Sterility Issues, United States

Sacred Tattoo Ink recalled due to Pseudomonas Aeruginosa Contamination, USA

Male Enhancement Dietary Supplements recalled due to Undeclared Ingredients, USA

Dexased™ and Dexmedvet™ Hydrochloride Injection recalled due to Particulate Matter, USA

Timed Release Melatonin recalled due to mislabelling, Canada

Tower Air Fryers recalled due to Risk of Fire, UK

Ropivacaine Hydrochloride Injection recalled due to Inert Fiber, USA

Bausch + Lomb Recalls enVista Intraocular Lenses Due to Safety Concern, USA

FDA Warns Against Inhalation of Nitrous Oxide Products Due to Health Risks, USA

CAPS Phenylephrine 40 mg recalled due to visible black particulate matter, USA

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