Create a Report

Please provide report title
Please provide location
  • 0:00 Processing...
Please provide details

Add more

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
Please provide email or phone

We do not show your email or contact info

Skip this step

Add photos or video

We recommend photos and videos to help explain your report

Add Photo/Video
Drop files here
Skip this step

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
Please provide email or phone

Thank you for your report!

The report was
successfully sent!

Edit my report

Your report is queued - it may take up to 12 hours to process your report.


Email us at support@safelyhq.com if you have questions.

Safety Reports: Recall

Updated:

Real Time Reports

Recall notice

Happy Hounds Wales Ltd raw dog food products - recalled because of potential Salmonella contamination, UK

5 years ago •source food.gov.uk • details

The FSA announced the recall of raw dog food products by Happy Hounds Wales Ltd because they may contain salmonella.

FSA advises consumers not to use the recalled product. Instead, return it to the store from where it was bought for a full refund. When handling and… See more

#recall #dogfood #petfood #unitedkingdom #beef #chicken

Recalls Happy Hounds Wales Ltd raw dog food products - recalled because of potential Salmonella contaminatio... photo #1
79   Comments Comment

Recall notice

Fresenius Kabi USA Dexmedetomidine HCL in 0.9% Sodium Chloride Injection - recalled due to cross contamination with Lidocaine, USA

5 years ago •source fda.gov • details

Company name: Fresenius Kabi USA
Brand name: Fresenius Kabi USA
Product recalled: Dexmedetomidine HCL in 0.9% Sodium Chloride Injection
Reason of the recall: Cross Contamination with Lidocaine
FDA Recall date: November 19, 2020
Recall details: Fresenius Kabi USA is voluntarily recalling a single lot of Dexmedetomidine HCl… See more

#crosscontamination #recall #drugs #unitedstates

Recalls Fresenius Kabi USA Dexmedetomidine HCL in 0.9% Sodium Chloride Injection - recalled due to cross con... photo #1
312   Comments Comment

Recall notice

Lohxa Chlorhexidine Gluconate Oral Rinse USP, 0.12% Alcohol free - recalled as it may be contaminated with Burkholderia lata, USA

5 years ago •source fda.gov • details

Company name: Lohxa, LLC
Brand name: Lohxa
Product recalled: Chlorhexidine Gluconate Oral Rinse USP, 0.12% Alcohol free
Reason of the recall: May be contaminated with Burkholderia lata
FDA Recall date: November 09, 2020
Recall details: Lohxa, LLC is voluntarily recalling Chlorhexidine Gluconate Oral Rinse USP, 0.12% Alcohol… See more

#recall #drugs #unitedstates

Recalls Lohxa Chlorhexidine Gluconate Oral Rinse USP, 0.12% Alcohol free - recalled as it may be contaminate... photo #1
312   Comments Comment

Recall notice

Nostrum Laboratories Metformin HCl Extended Release Tablets, USP 500 mg - recalled due to NDMA exceeds acceptable daily intake limit, USA

5 years ago •source fda.gov • details

Company name: Nostrum Laboratories
Brand name: Nostrum Laboratories
Product recalled: Metformin HCl Extended Release Tablets, USP 500 mg
Reason of the recall: NDMA exceeds acceptable daily intake limit
FDA Recall date: November 03, 2020
Recall details: Nostrum Laboratories, Inc. is voluntarily recalling 2 (two) lots of Metformin… See more

#blood #recall #drugs #unitedstates

312   Comments Comment

Recall notice

Nostrum Laboratories Metformin HCl Extended Release Tablets, USP 750 mg - recalled due to NDMA exceeds acceptable daily intake limit, USA

5 years ago •source fda.gov • details

Company name: Nostrum Laboratories
Brand name: Nostrum Laboratories
Product recalled: Metformin HCl Extended Release Tablets, USP 750 mg
Reason of the recall: NDMA exceeds acceptable daily intake limit
FDA Recall date: November 02, 2020
Recall details: Kansas City, Missouri, Nostrum Laboratories, Inc. is voluntarily recalling 2 (two)… See more

#blood #recall #drugs #unitedstates

312   Comments Comment

Recall notice

Eishindo Jelly Cups - recalled due to product poses a choking hazard., USA

5 years ago •source fda.gov • details

Company name: Hadson Toko Trading Co., Inc.
Brand name: Eishindo
Product recalled: Jelly Cups
Reason of the recall: Product poses a choking hazard.
FDA Recall date: October 14, 2020
Recall details: HADSON (TOKO) TRADING CO., INC. OF MASPETH, NY is recalling its 28.2oz (800g) bags of EISHINDO… See more

#recall #foodsafetyissue #unitedstates

Recalls Eishindo Jelly Cups - recalled due to product poses a choking hazard. Company name: Hadson Toko Trad... photo #1
312   Comments Comment

Recall notice

Time-Cap Labs Inc. Metformin Hydrochloride for Extended-Release Tablets, USP 500 mg and 700 mg - recalled due to the Detection of N-Nitrosodimethylamine (NDMA) Impurity, USA

5 years ago •source fda.gov • details

Company name: Marksans Pharma Limited
Brand name: Time-Cap Labs Inc.
Product recalled: Metformin Hydrochloride for Extended-Release Tablets, USP 500 mg and 700 mg
Reason of the recall: Due to the Detection of N-Nitrosodimethylamine (NDMA) Impurity
FDA Recall date: October 05, 2020
Recall details: Marksans Pharma Limited, India… See more

#blood #recall #drugs #unitedstates

Recalls Time-Cap Labs Inc. Metformin Hydrochloride for Extended-Release Tablets, USP 500 mg and 700 mg - rec... photo #1
312   Comments Comment

Recall notice

Riomet ER - recalled due to due to NDMA Impurity, USA

5 years ago •source fda.gov • details

Company name: Sun Pharmaceutical Industries
Brand name: Riomet ER
Product recalled: Metformin Hydrochloride for Extended-Release Oral Suspension
Reason of the recall: Due to the Detection of N-Nitrosodimethylamine (NDMA) Impurity
FDA Recall date: September 23, 2020
Recall details: Sun Pharmaceutical Industries, Inc. (SUN PHARMA), a wholly owned subsidiary… See more

#recall #drugs #unitedstates

Recalls Riomet ER - recalled due to due to NDMA Impurity Company name: Sun Pharmaceutical Industries Brand... photo #1
312   Comments Comment

Recall notice

Billy+Margot Wild Kangaroo and Superfoods Recipe Dog food - recalled due to Salmonella, USA

5 years ago •source fda.gov • details

Company name: Real Pet Food Company
Brand name: Billy+Margot Wild Kangaroo and Superfoods Recipe
Product recalled: Dog food
Reason of the recall: Salmonella
FDA Recall date: September 22, 2020
Recall details: Real Pet Food Company is voluntarily recalling Billy+Margot Wild Kangaroo and Superfoods Recipe 4lb bags because… See more

#recall #dogfood #animalveterinary #unitedstates

312   Comments Comment

Recall notice

BD Alaris System Hardware - recalled due to Potential for four hardware situations that may result in the infusion pump not operating as expected, USA

5 years ago •source fda.gov • details

Company name: Becton, Dickinson and Company
Brand name: Alaris
Product recalled: BD Alaris System Hardware
Reason of the recall: Potential for four hardware situations that may result in the infusion pump not operating as expected
FDA Recall date: September 21, 2020
Recall details: Three Recalls Designated as… See more

#recall #medicaldevices #unitedstates

312   Comments Comment

Popular topics

#Unordered Package #Scam #Facebook Scam #Cedar Grove #Las Vegas #DreamBone Dog Treats #Pet Food #Online Scam #Delivery #Starbucks #Drugs