Recall

McLarens and AXON Shake Up Claims Management in the Product Recall Market

Retrieved on: 
Monday, July 20, 2020
Food, Beverage, Retail, Professional services, Supermarket, Insurance, Legal professions, Actuarial science, Insurance, Claims adjuster, Service industries, Recall, Underwriting, Economy

Product recall claims tend to be low frequency, but high severity events and are typically not sufficient to allow for full-time product recall adjusters to staff an insurance carriers in-house team.

Key Points: 
  • Product recall claims tend to be low frequency, but high severity events and are typically not sufficient to allow for full-time product recall adjusters to staff an insurance carriers in-house team.
  • The joint AXON and McLarens claims administration program for product contamination and recall related claims provides access to 100% local product recall expertise, from underwriting to claims management.
  • It assures that their claims will receive local product recall claims expertise and decision-making in the evaluation and adjustment of claims which typically involve liquidity issues.
  • Product Recall/Contaminated Products Insurance claims are often complex, requiring specialized claims professionals, added Alex Pittignano, Senior Vice President at Axon Crisis Management Division.

4e Brands North America Issues Nationwide Voluntary Recall of Hand Sanitizer Due to Potential Presence of Undeclared Methanol (Wood Alcohol)

Retrieved on: 
Monday, July 13, 2020
Marketing, Merchandising, Articles, Economy, Consumer behaviour, Online shopping, Distribution, Product return, Recall, Retail, Brand

The product was distributed nationwide in the United States through retailers and distributors.

Key Points: 
  • The product was distributed nationwide in the United States through retailers and distributors.
  • 4e Brands North America is notifying its distributors and retailers by recall letter and consumers via this press release.
  • 4e Brands North America is arranging for the return and refund of all recalled products.
  • Consumers/distributors/retailers that have the product subject to this recall should stop using/distributing/selling Hand Sanitizer and return it to the place of purchase.

CME America Announces a Follow-Up on the Voluntary Recall of BodyGuard® Infusion System Administration Sets

Retrieved on: 
Friday, July 3, 2020
Life sciences, Medical technology, Medicine, Infusion set, Infusion pump, Becton Dickinson, Recall, Precision and recall

GOLDEN, Colo., July 3, 2020 /PRNewswire/ -- CME America, a wholly owned subsidiary of BD (Becton, Dickinson and Company), announced a voluntary recall for all CME America BodyGuard Infusion System Administration Sets (infusion sets)used with the company's BodyGuard infusion pumpsthat were distributed beginning May 2016 (see complete impacted product list below).

Key Points: 
  • GOLDEN, Colo., July 3, 2020 /PRNewswire/ -- CME America, a wholly owned subsidiary of BD (Becton, Dickinson and Company), announced a voluntary recall for all CME America BodyGuard Infusion System Administration Sets (infusion sets)used with the company's BodyGuard infusion pumpsthat were distributed beginning May 2016 (see complete impacted product list below).
  • As part of CME America's commitment to quality, following the previously announced recall (April 27, 2020) of the BodyGuard Infusion Pump Systems, the company conducted additional flow-rate accuracy testing.
  • This testing revealed that some infusion sets do not meet the 5% delivery accuracy for the system or the 13% accuracy identified in the earlier recall notification ( https://www.bd.com/en-us/support/recall-notifications/recall-notificatio... ).
  • Based on those test results CME America is providing additional information and customer actions regarding its previous recall to include all infusion sets used with the BodyGuard infusion pump distributed beginning May 2016.

Information Update - Certain Metformin diabetes drugs recalled due to the presence or possible presence of NDMA

Retrieved on: 
Saturday, June 13, 2020
RTT, Drugs, Health, Medicine, Metformin, National Disaster Management Authority, Diabetes management, Diabetes, Nitrosamine, 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.
  • NDMA test results are not available for this product; this recall has been initiated because of the potential presence of nitrosamine impurities in the finished product.
  • The risks from not having adequate diabetes treatment outweigh any possible effects of exposure to the levels of NDMA found in the recalled products.
  • The following is a list of metformin drugs being recalled in Canada at this time:

Local New-car Dealers Open for Free Safety Recall Repair

Retrieved on: 
Monday, June 8, 2020
Automotive safety, Motor vehicles, Transport, Land transport, Product recall, National Highway Traffic Safety Administration, Recall, 2009–11 Toyota vehicle recalls, Technical Service Bulletin

All safety recall work is performed free of charge, with many new-car dealers offering drop-off and pick-up service and loaner vehicles.

Key Points: 
  • All safety recall work is performed free of charge, with many new-car dealers offering drop-off and pick-up service and loaner vehicles.
  • Safety recalls are serious, and recall repairs are completely free.
  • A safety recall is issued when a manufacturer or the NHTSA determines that a vehicle creates an unreasonable safety risk or fails to meet minimum safety standards.
  • New-car dealerships have access to the proper procedures, parts and tools, ensuring that safety recall repairs are corrected properly.

FSIS Recall Release 011-2020 - Misbranding and Undeclared Allergen

Retrieved on: 
Friday, May 29, 2020
Food and drink, Articles, Food industry, Food Safety and Inspection Service, Food safety in the United States, Food safety, Recall, Chicken as food, Lean Cuisine

establishment, is recalling approximately 29,002 pounds of chicken product labeled as Lean Cuisine Fettuccini Alfredo because the product contains undeclared soy, a known allergen, the U.S. Department of Agricultures Food Safety and Inspection Service (FSIS) announced today.

Key Points: 
  • establishment, is recalling approximately 29,002 pounds of chicken product labeled as Lean Cuisine Fettuccini Alfredo because the product contains undeclared soy, a known allergen, the U.S. Department of Agricultures Food Safety and Inspection Service (FSIS) announced today.
  • The following products are subject to recall [ View Labels (PDF Only )]:
    9 1/4-oz.
  • The products subject to recall bear establishment number P27333 printed on the package next to the lot code.
  • Members of the media with questions about the recall can contact Kate Shaw, Nestl USA Corporate Communications, at [email protected] .

Government requests recall of Parliament

Retrieved on: 
Thursday, May 28, 2020
Parliament of Singapore, Recall, Speaker of the House of Commons, R (Miller) v The Prime Minister and Cherry v Advocate General for Scotland

The Speaker has written to MPs to explain why he has accepted the Government's request to recall Parliament.

Key Points: 
  • The Speaker has written to MPs to explain why he has accepted the Government's request to recall Parliament.
  • The Government has requested that the House be recalled for an earlier sitting on Tuesday 2 June 2020, to sit from 11.30am.
  • Now that I have agreed to a recall on Tuesday, it is for the Government to decide what proposal for voting it wishes to put forward.
  • It is for the Government to set out its proposals for the remaining business of the day.

Government requests recall of Parliament

Retrieved on: 
Thursday, May 28, 2020
Parliament of Singapore, Recall, Speaker of the House of Commons, R (Miller) v The Prime Minister and Cherry v Advocate General for Scotland

The Speaker has written to MPs to explain why he has accepted the Government's request to recall Parliament.

Key Points: 
  • The Speaker has written to MPs to explain why he has accepted the Government's request to recall Parliament.
  • The Government has requested that the House be recalled for an earlier sitting on Tuesday 2 June 2020, to sit from 11.30am.
  • Now that I have agreed to a recall on Tuesday, it is for the Government to decide what proposal for voting it wishes to put forward.
  • It is for the Government to set out its proposals for the remaining business of the day.

New Nootropic Gel by Healthycell Designed to Support Brain Health, Focus, and Recall

Retrieved on: 
Tuesday, May 19, 2020
Articles, Branches of biology, Medicine, Recycling industry, TerraCycle, Waste collection, Recycling, Nootropic, Recall, Ice pack, Antioxidant

VERONA, N.J., May 19, 2020 /PRNewswire/ -- Healthycell today announced the launch ofFocus + Recall, a new addition to its line of category-leading MICROGEL supplements.

Key Points: 
  • VERONA, N.J., May 19, 2020 /PRNewswire/ -- Healthycell today announced the launch ofFocus + Recall, a new addition to its line of category-leading MICROGEL supplements.
  • "Back in 2008, a Microsoft Corporation study showed people could spend 12 seconds on a concentrated task without becoming distracted.
  • Focus + Recall is the only nootropic gel on the market with neurotransmitters, adaptogens, cognitive fuel, brain blood flow support, and antioxidants that support optimal brain function.
  • Product boxes are recyclable through local municipal recycling programs, and gel packs are recyclable through the company's partnership with TerraCycle .

Hodedah Recalls HI4DR 4-Drawer Chests Due to Tip-Over and Entrapment Hazards; Remedies May Be Delayed Due to COVID-19 Restrictions; Keep Product Away from Children

Retrieved on: 
Wednesday, May 13, 2020
Individual Taxpayer Identification Number, Internal Revenue Service, ASTM International, Recall

The chests do not comply with the performance requirements of the U.S. voluntary industry standard (ASTM 2057-19).

Key Points: 
  • The chests do not comply with the performance requirements of the U.S. voluntary industry standard (ASTM 2057-19).
  • Consumers should immediately stop using any recalled chestthat is not properly anchored to the wall and place itin an area that children cannot access.
  • The chests measure about 40 inches tall, 27.5 inches wide, and 15.5 inches deep and weigh about 84 pounds.
  • Contact us at this toll-free number if you have questions about a recall:
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