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Safety Reports: Recall

Updated: April 20, 2025 9:59 AM

Real Time Reports

Recall notice

Tower Air Fryers recalled due to Risk of Fire, UK

11 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

11 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

1 year 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

1 year 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

#drugs #recall #unitedstates

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SinuCleanse Soft Tip Squeeze Bottle Nasal Wash System recalled due to Staphylococcus aureus, USA

1 year ago •source fda.gov • details

Ascent Consumer Products Inc. is voluntarily recalling one lot of SinuCleanse Soft Tip Squeeze Bottle Nasal Wash System to the consumer level. The recall is being initiated due to a confirmed test result of microbial contamination of the product with Staphylococcus aureus (S. aureus). The affected lot… See more

#drugs #recall #unitedstates

Recalls SinuCleanse Soft Tip Squeeze Bottle Nasal Wash System recalled due to Staphylococcus aureus Ascent C... photo #1

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Recall notice

Vitality male enhancement dietary supplement capsules recalled due to Undeclared Ingredients, USA

1 year ago •source fda.gov • details

One Source Nutrition is voluntarily recalling all lots of Vitality capsules to the Consumer level. FDA analysis has found the product to be tainted with sildenafil and tadalafil, which are ingredients in FDA-approved products for the treatment of male erectile dysfunction in the family of drugs known… See more

#recall #unitedstates

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Recall notice

ICU Medical POTASSIUM CHLORIDE Inj. recalled due to Mislabeling, USA

1 year ago •source fda.gov • details

ICU Medical, Inc. is voluntarily recalling one lot each of POTASSIUM CHLORIDE Inj. bags with overwrap labels 10mEq, packaged in cases of POTASSIUM CHLORIDE Inj. 20 mEq, to the user level. ICU Medical has received a customer complaint which states that bags of POTASSIUM CHLORIDE Inj. 20… See more

#recall #unitedstates

Recalls ICU Medical POTASSIUM CHLORIDE Inj. recalled due to Mislabeling ICU Medical, Inc. is voluntarily rec... photo #1

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Recall notice

Olympus MAJ-891 endoscope accessory recalled due to risk of contamination, USA

1 year ago •source fda.gov • details

Olympus Corporation has announced a voluntary Advisory Notice for the Forceps/Irrigation Plug (Isolated Type) model MAJ-891 related to the risk of device contamination that may result from improper reprocessing of the MAJ-891 accessory. The MAJ-891 is an endoscope accessory attached to the instrument channel port of certain… See more

#medicaldevices #recall #unitedstates

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Phenylephrine hydrochloride Injection, USP, 10 mg/ mL recalled due to Potential Foreign Material, USA

1 year ago •source fda.gov • details

Provepharm Inc. is voluntarily recalling lot number 24020027; Expiry Date December 2025 of Phenylephrine hydrochloride Injection, USP, 10 mg/ mL (Pharmacy Bulk Package) at the hospital/institutional level. This recall was initiated based on a customer complaint from a pharmacy after observing a visible black particulate matter found… See more

#drugs #recall #unitedstates

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Safety Reports: Recall

Real Time Reports

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

SinuCleanse Soft Tip Squeeze Bottle Nasal Wash System recalled due to Staphylococcus aureus, USA

Vitality male enhancement dietary supplement capsules recalled due to Undeclared Ingredients, USA

ICU Medical POTASSIUM CHLORIDE Inj. recalled due to Mislabeling, USA

Olympus MAJ-891 endoscope accessory recalled due to risk of contamination, USA

Phenylephrine hydrochloride Injection, USP, 10 mg/ mL recalled due to Potential Foreign Material, USA

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