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: July 22, 2024 6:03 PM

Real Time Reports

Recall notice

Hikma Acetaminophen Injection - recalled due to Dexmedetomidine HCL presence, USA

1 year ago •source fda.gov • details

Hikma Pharmaceuticals USA, Inc. is voluntarily recalling one lot of Acetaminophen Injection to the consumer/user level. The product is being recalled due to the potential presence of a bag labeled Dexmedetomidine HCL Injection (400mcg/100mL) inside the overwrap that is labeled Acetaminophen Injection, 1000mg/100mL, (10mg/mL). The product was… See more

#recall #drugs #unitedstates

Recalls Hikma Acetaminophen Injection - recalled due to Dexmedetomidine HCL presence Hikma Pharmaceuticals U... photo #1

312

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

Clonazepam Orally Disintegrating Tablets - recalled due to Mislabeling, USA

1 year ago •source fda.gov • details

Endo USA, Inc. is voluntarily recalling one lot of Clonazepam Orally Disintegrating Tablets to the consumer level. The product lot is being recalled due to mislabeling where an incorrect strength appears on the cartons. The product lot was distributed through wholesale distributors to retail pharmacies nationwide.

Risk… See more

#recall #drugs #unitedstates

Recalls Clonazepam Orally Disintegrating Tablets - recalled due to Mislabeling Endo USA, Inc. is voluntarily... photo #1

312

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

Volara System Single-Patient Use Circuit and Blue Ventilator Adapter recalled for Handset Plug Issue, USA

1 year ago •source fda.gov • details

Baxter International Inc. issued an Urgent Medical Device Recall for certain lots of the Volara system single-patient use circuit and blue ventilator adapter assembly. The recall is due to reports of the handset plug disconnecting from the nebulizer port on the blue ventilator adapter. The impacted accessories… See more

#recall #medicaldevices #unitedstates

Recalls Volara System Single-Patient Use Circuit and Blue Ventilator Adapter recalled for Handset Plug Issue... photo #1

312

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

Infla-650 Herbal Dietary Supplement Capsules - recalled due to undeclared drug ingredients, USA

1 year ago •source fda.gov • details

GURU INC. is voluntarily recalling Infla-650 Herbal Dietary Supplement Capsules, Lot No. IN-032, 700 mg to the consumer/user level. Infla-650 capsules has been found to be tainted with acetaminophen, diclofenac and phenylbutazone, which are not listed on the label. Products containing acetaminophen, diclofenac and phenylbutazone cannot be… See more

#drugs #recall #dietarysupplements #unitedstates

Recalls Infla-650 Herbal Dietary Supplement Capsules - recalled due to undeclared drug ingredients GURU INC.... photo #1

312

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

Umary Acido Hialuronica Capsules - recalled due to Undeclared Drug Ingredients, USA

1 year ago •source fda.gov • details

SoloVital.com is voluntarily recalling all lots of Umary Acido Hialuronica, Suplemento Alimenticio – 30 Capletas de 850mg to the consumer level. FDA laboratory analysis confirmed that UMARY has been found to be tainted with the drug ingredients, diclofenac and omeprazole. Products containing diclofenac and omeprazole drug cannot… See more

#recall #drugs #unitedstates

Recalls Umary Acido Hialuronica Capsules - recalled due to Undeclared Drug Ingredients SoloVital.com is volu... photo #1

312

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

Hard Steel Capsules & Gold Hard Steel Plus Liquid recalled due to Sildenafil and Acetaminophen, USA

1 year ago •source fda.gov • details

Supercore Products Group is voluntarily recalling of Hard Steel Capsules & Gold Hard Steel Plus Liquid to the consumer level. FDA analysis has found these products to be tainted with Sildenafil and acetaminophen. Hard Steel is sold worldwide online via their website.

Risk Statement: Consumption of products… See more

#recall #dietarysupplements #unitedstates

Recalls Hard Steel Capsules & Gold Hard Steel Plus Liquid recalled due to Sildenafil and Acetaminophen Supe... photo #1

312

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

Baxter Life2000 Ventilator - recalled due to battery charger dongle damage, USA

1 year ago •source fda.gov • details

Baxter International Inc. announced today it has issued an Urgent Medical Device Recall for Life2000 ventilators with an attached battery charger dongle. The recall is due to reports that the devices are not properly charging when there is damage to the battery charger dongle. The impacted ventilators… See more

#recall #medicaldevices #unitedstates

Recalls Baxter Life2000 Ventilator - recalled due to battery charger dongle damage Baxter International Inc.... photo #1

312

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

Viva Raw dog and cat food - recalled due to listeria monocytogenes, USA

1 year ago •source fda.gov • details

Viva Raw LLC is voluntarily recalling dog and cat foods due to listeria monocytogenes. The products were distributed directly to consumers in all fifty states and the District of Columbia.

Listeria monocytogenes can cause serious and sometimes fatal infections in pets eating contaminated products. People can become… See more

#recall #petfood #unitedstates

Recalls Viva Raw dog and cat food - recalled due to listeria monocytogenes Viva Raw LLC is voluntarily recal... photo #1

312

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

Sunseed Vita Prima Hedgehog Food - recalled due to salmonella, USA

1 year ago •source fda.gov • details

Vitakraft Sun Seed Inc. is working closely with the FDA and MN Department of Agriculture and out of an abundance of caution has elected to expand the recall to include the following lots of Sun Seed Vita Prima Hedgehog Food and Vitakraft Vita Smart Hedgehog Food because… See more

#recall #petfood #unitedstates

Recalls Sunseed Vita Prima Hedgehog Food - recalled due to salmonella Vitakraft Sun Seed Inc. is working clo... photo #1

312

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

Potassium Chloride Extended Release Capsules - recalled due to Failed dissolution, USA

1 year ago •source fda.gov • details

American Health Packaging on behalf of BluePoint Laboratories is voluntarily recalling 21 batches of Potassium Chloride Extended-Release Capsules, USP (750 mg) 10 mEq K, to the consumer level. The product is being recalled because of failed dissolution. The Potassium Chloride Extended-Release Capsules being recalled were distributed nationwide… See more

#recall #drugs #unitedstates

Recalls Potassium Chloride Extended Release Capsules - recalled due to Failed dissolution American Health Pa... photo #1

312

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

Hikma Acetaminophen Injection - recalled due to Dexmedetomidine HCL presence, USA

Clonazepam Orally Disintegrating Tablets - recalled due to Mislabeling, USA

Volara System Single-Patient Use Circuit and Blue Ventilator Adapter recalled for Handset Plug Issue, USA

Infla-650 Herbal Dietary Supplement Capsules - recalled due to undeclared drug ingredients, USA

Umary Acido Hialuronica Capsules - recalled due to Undeclared Drug Ingredients, USA

Hard Steel Capsules & Gold Hard Steel Plus Liquid recalled due to Sildenafil and Acetaminophen, USA

Baxter Life2000 Ventilator - recalled due to battery charger dongle damage, USA

Viva Raw dog and cat food - recalled due to listeria monocytogenes, USA

Sunseed Vita Prima Hedgehog Food - recalled due to salmonella, USA

Potassium Chloride Extended Release Capsules - recalled due to Failed dissolution, 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!