Recall | Jotup

Advisory - Certain lots of antidepressant drug APO-Amitriptyline recalled because of nitrosamine impurity

Retrieved on:

Friday, April 30, 2021

Pharmaceutical companies, Apotex, Recall, Companies, Health care, Ranitidine

b'Issue:Apotex Inc. is recalling certain lots because of a nitrosamine impurity.\nWhat to do:Patients can continue to take their medication as prescribed by their health care provider asthere is no immediate risk in continuing to take the recalled medication.

Key Points:

b'Issue:Apotex Inc. is recalling certain lots because of a nitrosamine impurity.\nWhat to do:Patients can continue to take their medication as prescribed by their health care provider asthere is no immediate risk in continuing to take the recalled medication.
The affected products table below has been updated with information on the recall.
This means that long-term exposure to a level above what is considered safe may increase the risk of cancer.
Should any additional recalls be deemed necessary, Health Canada will update the table below and inform Canadians.\n'

BD Announces the Voluntary Recall of Specified Lots of ChloraPrep™ Hi-Lite Orange™ 26 mL Applicator in the United States and U.S. Territories Due to Defective Applicator

Retrieved on:

Tuesday, April 20, 2021

Spanish Empire, Applicator, Recall, PUERTO RICO, Countries, Islands

In certain lots, the applicator end cap was improperly secured due to a manufacturing error.

Key Points:

In certain lots, the applicator end cap was improperly secured due to a manufacturing error.
This can result in broken glass and solution dropping out of the applicator once activated.
These products were distributed in the United States and Puerto Rico.\nImmediate health consequences could be lacerations to patient and/or user of the device.
BD\'s Customer Recall Notification provides instructions to customers and distributors for disposal and replacement of the impacted ChloraPrep Hi-Lite Orange 26 mL Applicator (see list of affected lot numbers below).\n'

BD Expands Voluntary Class I Recall of ChloraPrep™ 3 mL Applicator to Include All U.S. States

Retrieved on:

Saturday, March 20, 2021

Food and Drug Administration, United States Public Health Service, Recall, Health, Food recalls, Dietary Supplements, Biology

There has been noidentified risk associated with thesterile ChloraPrep antiseptic solution within the applicator.

Key Points:

There has been noidentified risk associated with thesterile ChloraPrep antiseptic solution within the applicator.
Out of an abundance of caution and in consultation with the U.S. Food and Drug Administration (FDA), BD has expanded the recall to include all U.S. states.
To date, no complaints, adverse events, injuries, or deaths have been reported related to this voluntary recall.
As part of the voluntary recall to the user level, the companywill notifycustomers and distributors affected by the recall.

Aki-Home Recalls Some Bath Mats, Drink Coasters

Retrieved on:

Wednesday, March 17, 2021

Industrial Minerals, Floors, Physical sciences, Earth sciences, Academic disciplines, Occupational safety and health, Beer advertising, Drink coaster, Ephemera, Recall, Asbestos, Mat

ONTARIO, Calif., March 17, 2021 (GLOBE NEWSWIRE) -- Aki-Home is recalling certain bath mats and drink coasters, a small number of which were purchased by U.S. customers, primarily in Southern California.

Key Points:

ONTARIO, Calif., March 17, 2021 (GLOBE NEWSWIRE) -- Aki-Home is recalling certain bath mats and drink coasters, a small number of which were purchased by U.S. customers, primarily in Southern California.
Although fewer than 25 bath mats and fewer than 125 drink coasters are involved, the recall is proceeding out of an abundance of caution and to demonstrate Aki-Homes commitment to always place its customers interests first.
The recall is being conducted voluntarily and independently (although with the knowledge) of U.S. government agencies.
The recall is because of a manufacturing error that, unbeknownst to Aki-Home, some diatomaceous products from a now-defunct manufacturer contained minute amounts of asbestos.

Sedgwick's brand protection experts publish the highly anticipated European recall index report

Retrieved on:

Thursday, March 4, 2021

Recall

This industry leading research and analysis were designed and delivered by Sedgwick's experts in best practice recall, remediation and retention solutions.

Key Points:

This industry leading research and analysis were designed and delivered by Sedgwick's experts in best practice recall, remediation and retention solutions.
Food and beverage recalls decreased only 6%, owing to better food handling and hygiene practices as a direct outcome of COVID-19.
Pharmaceutical recalls dropped 40%, partly due to global research being paused and efforts switched to the fight against COVID-19.
The recall index is produced by Sedgwick's brand protection experts every quarter.

FSIS Recall Release 005-2021 - Without Inspection

Retrieved on:

Friday, February 19, 2021

Food Safety and Inspection Service, Food safety in the United States, Meat inspection, Food and drink, Pork, Recall

The following heat-treated shelf stable pork pt items are subject to recall:

Key Points:

The following heat-treated shelf stable pork pt items are subject to recall:
The products subject to recall bear the French establishment number FR 56-246-008 CE, an ineligible establishment.
There have been no confirmed reports of adverse reactions due to consumption of these products.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers.
When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls .

Agero Introduces End-to-End Vehicle Recall Management Solution, Helping Auto Manufacturers Quickly and Effectively Drive Recall Completion

Retrieved on:

Thursday, February 18, 2021

Software, Mobile, Wireless, Internet, Professional services, Data management, General Automotive, Technology, Automotive, Insurance, Automotive Manufacturing, Other Technology, Manufacturing, Recall, Brand, Marketing, Articles, Business

Agero , a market leader in software-enabled driver assistance services, today introduced Recall Solutions, the industrys first suite of integrated end-to-end vehicle recall management services.

Key Points:

Agero , a market leader in software-enabled driver assistance services, today introduced Recall Solutions, the industrys first suite of integrated end-to-end vehicle recall management services.
As vehicles and their systems grow in complexity and increasingly share components across models and brands, the industry continues to face frequent, high-impact recall campaigns.
Locating and reaching current owners can be difficult, and effectively coordinating across dealer and repair networks often becomes a logistical nightmare.
Agero, a member company of The Cross Country Group, is headquartered in Medford, Mass., with operations throughout North America and Europe.

NZXT Recalls H1 Computer Cases Due to Fire Hazard

Retrieved on:

Friday, February 12, 2021

NZXT, Recall, Computer case, Technology, Computing, Electronics industry

Consumers should immediately stop using the recalled computer cases and contact NZXT for a free repair kit.

Key Points:

Consumers should immediately stop using the recalled computer cases and contact NZXT for a free repair kit.
This recall involves NZXT H1 computer cases with model numbers CA-H16WR-W1 (matte white) and CA-H16WR-B1 (matte black) and serial numbers 1200233400001 to 1203962204202, 00648999610844189725 to 00648999610844206361, and 0120AC00100001 to 01211C01900285.
The computer cases have a black tempered glass front with the NZXT brand name at the bottom.
Fast Track recalls are initiated by firms who commit to work with CPSC to quickly announce the recall and remedy to protect consumers.

Information Update - Ranitidine products recalled because of a nitrosamine impurity

Retrieved on:

Friday, February 5, 2021

Chemistry, Hepatotoxins, Health, Drugs, Furans, Ranitidine, Thioethers, Over-the-counter drug, Pharmascience, Nitrosamine, National Disaster Management Authority, Recall

Please refer to the Affected Products table below for detailed information on the recalled lots.

Key Points:

Please refer to the Affected Products table below for detailed information on the recalled lots.
Pharmascience Inc. is recalling 13 additional lots of its over-the-counter ranitidine products (75 mg strength tablet) after tests found NDMA, a nitrosamine impurity, above accepted levels.
Please refer to the Affected Products table below for detailed information on the recalled lots.
Please refer to the Affected Products table below for detailed information on the recalled lot (lot 619003).

Information Update - Ranitidine products recalled because of a nitrosamine impurity

Retrieved on:

Saturday, January 30, 2021

Hepatotoxins, Chemical compounds, Furans, Ranitidine, Thioethers, Drugs, Organic compounds, Recall

Please refer to the Affected Products table below for detailed information on the recalled lots.

Key Points:

Please refer to the Affected Products table below for detailed information on the recalled lots.
Please refer to the Affected Products table below for detailed information on the recalled lots.
Please refer to the Affected Products table below for detailed information on the recalled lot (lot 619003).
The following is a list of ranitidine products being recalled in Canada at this time.