Create a Report

Please provide report title

Please provide location

Please provide details

Make my report private

Alert regulators Alert business or product owner Get notifications for my case

Get alerts and updates for your case!

This information is not shown on the website. We can notify you of updates, and may contact you for more information to help resolve or follow up on your issue.

Please provide email or phone

Phone Number

Please provide email or phone

Show my report on homepage

We do not show your email or contact info

Skip this step

I agree to Terms & Conditions

Please accept our Terms & Conditions

Email or SMS copy of report

Enter below to get emailed a copy of your report, or sms a link to your report

Please provide email or phone

Phone number

Please provide email or phone

I agree to Terms & Conditions

Please accept our Terms & Conditions

Safety Reports: Recall

Updated: April 20, 2025 9:59 AM

Real Time Reports

Recall notice

Timed Release Melatonin recalled due to mislabelling, Canada

8 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

87

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

Tower Air Fryers recalled due to Risk of Fire, UK

8 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

166

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

Ropivacaine Hydrochloride Injection recalled due to Inert Fiber, USA

8 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

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

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

9 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

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

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

10 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

17

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

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

10 months 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

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

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

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

10 months 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

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

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

10 months 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

Recalls Vitality male enhancement dietary supplement capsules recalled due to Undeclared Ingredients One Sou... photo #1

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

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

10 months 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

16

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

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

11 months 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

Recalls Olympus MAJ-891 endoscope accessory recalled due to risk of contamination Olympus Corporation has an... photo #1

Helpful
Follow
Add my report
Share
- Copy link

Create a Report

Get alerts and updates for your case!

Add photos or video

Email or SMS copy of report

Thank you for your report!

Safety Reports: Recall

Real Time Reports

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

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

I have a concern about this report:

Resolve my concern fast!

Thanks for your feedback!

Notify me when my concern is resolved

Thanks for your feedback!

Create a Report

Get alerts and updates for your case!

Add photos or video

Email or SMS copy of report

Thank you for your report!

Real Time Reports

Country

Type

Date

I have a concern about this report:

Resolve my concern fast!

Thanks for your feedback!

Notify me when my concern is resolved

Thanks for your feedback!