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: February 25, 2025 3:02 PM

Real Time Reports

Recall notice

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

#recall #drugs #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

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

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

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

16

Helpful
Follow
Add my report
Share
- Copy link

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

#recall #medicaldevices #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

Recall notice

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

#recall #drugs #unitedstates

Recalls Phenylephrine hydrochloride Injection, USP, 10 mg/ mL recalled due to Potential Foreign Material Pro... photo #1

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

Aactive D3 supplements recalled due of excess levels of Vitamin D3, UK

1 year ago •source data.food.gov.uk • details

TriOn Pharma is recalling two food supplement products. Aactive D3 Drops and Aactive D3 Solution because they contain higher levels of vitamin D3 than written on the label.

Product details:
- Product Name: Aactive D3 2,000iu/ml Oral Drops, Pack size: (20ml), Batch code: LS23317, Best before: November… See more

#vitamins #recall #unitedkingdom

Recalls Aactive D3 supplements recalled due of excess levels of Vitamin D3 TriOn Pharma is recalling two foo... photo #1

163

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

Astellas Tacrolimus and Tacrolimus Extended-Release capsules - recalled due to Bottles may contain empty capsules., USA

1 year ago •source fda.gov • details

Astellas Pharma US, Inc. is voluntarily recalling one lot of PROGRAF® 0.5mg (tacrolimus) and one lot of ASTAGRAF XL® 0.5mg (tacrolimus extended-release) capsules to the consumer level. These products are being recalled because bottles may contain empty capsules. The product was distributed nationwide to wholesale and retail… See more

#recall #drugs #unitedstates

Recalls Astellas Tacrolimus and Tacrolimus Extended-Release capsules - recalled due to Bottles may contain e... photo #1

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

Systane Lubricant Eye Drugs - recalled due to Fungal Contamination, USA

1 year ago •source fda.gov • details

Alcon Laboratories is voluntarily recalling one (1) lot of Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, 25 count to the consumer level. Alcon evaluated a consumer complaint of foreign material observed inside a sealed single use vial and determined the material to be fungal in… See more

#recall #drugs #unitedstates

Recalls Systane Lubricant Eye Drugs - recalled due to Fungal Contamination Alcon Laboratories is voluntarily... photo #1

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

Par Pharmaceutical Adrenalin® Chloride Solution recalled due to an unapproved drug, USA

1 year ago •source fda.gov • details

Endo USA, Inc., is voluntarily recalling all lots within expiry of Adrenalin® Chloride Solution (EPINEPHrine nasal solution, USP) 30mg/30mL (1mg/mL) 30 mL vials, to the consumer level. This product, which pre-dates the 1938 Federal Food, Drug & Cosmetic Act, was never submitted for approval by the FDA,… See more

#recall #drugs #unitedstates

Recalls Par Pharmaceutical Adrenalin® Chloride Solution recalled due to an unapproved drug Endo USA, Inc., i... photo #1

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

Fouzee SugarLin Herbal Dietary Supplement recalled due to Metformin and Glyburide, USA

1 year ago •source fda.gov • details

Shoppers-Plaza is voluntarily recalling all lots of Fouzee Sugarlin Herbal Formula capsules to the consumer level. Fouzee Sugarlin Herbal Formula capsules is an unapproved new drug for which safety and efficacy have not been established and, therefore, subject to recall. This product was promoted and sold nationwide… See more

#recall #drugs #unitedstates

Recalls Fouzee SugarLin Herbal Dietary Supplement recalled due to Metformin and Glyburide Shoppers-Plaza is... 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

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

Aactive D3 supplements recalled due of excess levels of Vitamin D3, UK

Astellas Tacrolimus and Tacrolimus Extended-Release capsules - recalled due to Bottles may contain empty capsules., USA

Systane Lubricant Eye Drugs - recalled due to Fungal Contamination, USA

Par Pharmaceutical Adrenalin® Chloride Solution recalled due to an unapproved drug, USA

Fouzee SugarLin Herbal Dietary Supplement recalled due to Metformin and Glyburide, 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!