Mock Recall Planning - Page 2 of 4 - mock recall planning procedures services

Researching Recall Management Software to Conduct Mock Recalls?

A product recall is a complicated process – not only are you working on tracking and fixing the problem throughout your supply chain, but you also need to coordinate communications with the media, government, public, and more. It quickly overwhelms a company that is not prepared for it, and that’s why recall management software [...]

Researching Recall Management Software to Conduct Mock Recalls?2022-06-06T20:03:05+00:00

Mock Recall Checklist

Review the Mock Recall checklist for your mock recall manual. Statement of Product Quality and Safety Procedure for maintenance of Recall Manual Relevant regulations and regulatory authority identified Organizational training requirements identified Mock recall requirements identified Recall Team members identified with contact information Roles and responsibilities identified for team and related functions Procedures [...]

Mock Recall Checklist2022-06-07T15:22:41+00:00

12 Steps to Take During a Mock Product Recall

All companies that distribute physical products are required to have a product recall plan. If it comes to your attention that a number of the same product is giving customers negative or unsafe results, it is important that you take action so that your company and goods can keep a positive reputation by only [...]

12 Steps to Take During a Mock Product Recall2022-05-31T14:59:30+00:00

Medical Device Model Recall Press and News Release Template

Published by the FDA under Industry Guidance for Recalls Note: Text in bold should be modified to reflect appropriate company information Company Name Issues Nationwide Recall of Product(s) Name(s) FOR IMMEDIATE RELEASE: Date of News Release Company Address Telephone/Company Website On date of recall initiation, Company Name initiated a nationwide recall of quantity and name of product(s). The product(s) have been [...]

Medical Device Model Recall Press and News Release Template2022-08-29T20:36:26+00:00

Expedited Medical Device Review Leads to More Recalls

The United States Food and Drug Administration has provided expedited priority review for certain medical devices since 1994. The move is meant to shorten the lead time it takes for patients to access breakthrough devices. However, new research published in JAMA Internal Medicine seems to draw correlations between shorter review times and increased chances [...]

Expedited Medical Device Review Leads to More Recalls2022-06-06T20:03:14+00:00

How to Conduct a Mock Recall for Cosmetics

Cosmetics recalls are an unfortunate reality that can negatively impact any business. The U.S. Food and Drug Administration is in charge of enforcing and monitoring recalls. There may have been a temporary lull in recall activity during the COVID-19 lockdowns, but it’s soon going to become the way of life, as the agency catches [...]

How to Conduct a Mock Recall for Cosmetics2022-06-06T20:03:25+00:00

Pitfalls to Look Out for in an Effective Product Recall Plan

An effective product recall plan involves multiple levels of consideration. These range from PR matters to staff mobilization and stock retrieval. Multi-faceted recall processes pose many pitfalls that might prove problematic for companies if poorly managed. The New Normal could worsen recall woes for various industries (i.e., foodstuff and healthcare) as regulatory bodies like [...]

Pitfalls to Look Out for in an Effective Product Recall Plan2022-06-06T20:03:35+00:00

Why Product Recalls Cost Medical Device Manufacturers $5,000,000 a Day

Researching and developing a medical breakthrough is easy when you compare it to the process of getting approval from the U.S. Food and Drug Administration. The FDA had a long list of requirements to reach and maintain compliance, and it’s not a cheap or easy process. Failing to do so, however, can cost your [...]

Why Product Recalls Cost Medical Device Manufacturers $5,000,000 a Day2022-06-06T20:03:54+00:00

How to Meet FDA Medical Device Recall Requirements

The last thing you need to deal with is a medical device recall. Whether a correction or complete removal from the market, a single medical device recall can cost up to $600 million. The U.S. Food and Drug Administration (FDA) has strict guidance on how and when a recall should be initiated. It’s a [...]

How to Meet FDA Medical Device Recall Requirements2022-06-06T20:04:03+00:00

7 KEY REASONS TO DIGITIZE YOUR RECALL MANAGEMENT PROCESS

Good news for retailers - the U.S. Consumer Product Safety Commission (CPSC) reports product recalls are at their lowest level in 16 years, with only 241 recalls. Even better, digital recall response can drastically reduce processing times and resources dedicated to recall management. Learn the 7 KEY REASONS TO DIGITIZE YOUR RECALL MANAGEMENT PROCESS. [...]

7 KEY REASONS TO DIGITIZE YOUR RECALL MANAGEMENT PROCESS2022-06-06T20:04:14+00:00