VOLUNTARY RECALLS
India Inc warms up to the idea of product recalls as pharma, auto industries lead the charge
In FY23, 30 companies undertook voluntary product recalls, while 16 were forced to recall their products, shows data sourced from Prime Database. Product recall information forms part of the business responsibility and sustainability reporting (BRSR) framework that is mandatory disclosure for the top 1,000 listed companies from FY23. Since many companies have not disclosed data for FY22, a YoY comparison is not tenable.
Hyundai and Kia to recall nearly 170,000 EVs over software problem in South Korea
HYUNDAI MOTOR-KIA CORP/EV-RECALL (UPDATE 1, PIX)UPDATE 1-Hyundai and Kia to recall nearly 170,000 EVs over software problem in South Korea
Do you own a Kia Seltos? The company is recalling some cars. Check details here
Kia India is recalling 4,358 petrol-powered Seltos SUVs due to a potential issue with the electronic oil pump controller. This could affect the performance of the automatic transmission.
India Yamaha Motor recalls 3 lakh scooter units to rectify brake parts
India Yamaha Motor is recalling approximately 300,000 units of its 125 cc scooter models Ray ZR 125 Fi Hybrid and Fascino 125 Fi Hybrid due to faulty brake parts. The recall applies to scooters manufactured between January 1, 2022, and January 4, 2024. Yamaha is providing free replacement parts to affected customers and has urged them to check their eligibility for the recall on the company's website or visit a Yamaha service center for assistance.
Sun Pharma, Lupin recall drugs in US market: USFDA
Sun Pharmaceutical is recalling the affected lot that was produced at the drugmaker's Dadra-based facility. The company is recalling the lot due to "failed impurities/degradation specifications", the USFDA stated. USFDA stated that Mumbai-based Lupin is also recalling an unspecified number of penicillamine tablets in the US.
Kraft food recalls American cheese slices as a ‘precaution’; Here’s what happened
In an official statement issued by Kraft Foods, it said that the recall was a precautionary measure due to a “temporary issue”.
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DCGI issues advisory as US-based Abbott recalls batches of Digene gel
Abbott India Limited, through a letter dated August 18, intimated to DCGI regarding voluntary product recall of all batches of Digene Gel of all flavours (mint, orange, mix fruits flavour) which are within the shelf life and manufactured at Goa facility. "The impugned product may be unsafe and its use may result in adverse reaction," the DCGI letter dated August 31 said.
DCGI issues advisory against Digene Gel; raises safety concerns after Abbott's voluntary recall
The Drugs Controller General of India has advised patients and healthcare professionals to stop using Digene gel, a popular antacid, due to safety concerns. The advisory comes after drugmaker Abbott initiated a voluntary recall of the product. Doctors and healthcare professionals are urged to carefully prescribe and inform their patients to stop using it.
Why has TOMY International recalled its Boon Highchairs: Model numbers, and key information
TOMY International Inc. has issued a product recall for its 'Boon Flair & Flair Elite highchairs out of safety concerns. These highchairs, which are suspected to have a detachment issue, were distributed in both the United States and Canada.
Alembic, Aurobindo recall drugs in US market
Alembic Pharmaceuticals and Aurobindo Pharma are recalling products in the US due to manufacturing problems. Alembic is recalling 82,400 bottles of Tobramycin Ophthalmic Solution due to “Failed Impurities/Degradation Specifications.” Meanwhile, Aurobindo Pharma is recalling 48 bottles of Rufinamide Tablets, in both 200 mg and 400 mg doses, due to cGMP (current good manufacturing practice) deviations, USFDA said. The batch was released prior to approval. Rufinamide tablets are used to treat seizure disorders.
Nikola recalls 209 battery-EV trucks over fire concerns
Nikola Motors has issued a voluntary recall of 209 battery-electric trucks 'Tre BEV' due to a coolant leak in a single battery pack which likely caused the fire at its headquarters. The company recommended that customers immediately place the Main Battery Disconnect switch on to enable safety systems operation and that they park the trucks outside to allow for over-the-air updates and better connectivity with Fleet Command.
Kia India recalls over 30,000 units of Carens for software update
The company has initiated the recall campaign for vehicle inspection and, if required, a free-of-cost software update is also provided, it added. The company conducts regular checks and rigorous testing of components, governed by brand's global standard, Kia India said in a statement. During this campaign, the company will take utmost care to minimise inconvenience to customers, it added.
Bags of frozen fruit recalled due to listeria contamination, including products sold at Walmart, Target, and Aldi
Several brands of frozen fruit, widely available at major retailers such as Walmart, Target, Aldi, Whole Foods, Trader Joe's, and AWG, are being voluntarily recalled due to possible listeria contamination.
Millions of Baby Shark Bath Toys recalled due to injury risk, CPSC announces
The CPSC has specifically recalled Baby Shark and Mini Baby Shark Bath Toys featuring hard plastic top fins, manufactured by Zuru.
Pfizer recalls three anti-bacterial injections in India manufactured by Astral SteriTech
The company was informed by its contract manufacturer in India, Astral, that it has observed an out-of-specification during a routine environmental monitoring of its manufacturing block, company said.
Abbott India recalls batch of Thyronorm due to labelling error
"This is due to a labelling error in a small percentage of bottles from this batch which has been mislabeled with the dose strength as 25 mcg, whereas the bottles contain 88 mcg tablets," the drug maker stated. The batch has been invoiced only in Madhya Pradesh and Telangana, it added.
GM's self-driving car crashes into bus, automaker recalls 300 robotaxis
The Cruise self-driving software failed to accurately predict the movement of the bus and struck the back after "decelerating too late to avoid a rear-end collision with the bus". Kyle Vogt, Cruise Founder and CEO, said that "fender benders like this rarely happen to our AVs, but this incident was unique."
HMSI recalls around 2K CB300R bike units
The company has identified that due to an inappropriate manufacturing process of the right crankcase cover of the engine, there are chances of sealing plug dislodging due to low retention force caused by engine heat, Honda Motorcycle & Scooter India said in a statement.
Ola offers to replace S1 scooter part amid safety concerns raised by customers
The company said recently there have been concerns amongst its users around the safety of its front fork arm, a key component between the body of the vehicle to its wheel.
Toyota Kirloskar to recall around 1,000 units of Urban Cruiser Hyryder
The automaker announced in a statement that there will be a voluntary recall campaign for 994 Urban Cruiser Hyryder units to investigate for a possible issue with front seat belt shoulder height adjuster plate assembly.
Dr Reddy's, Sun Pharma recall products in US for manufacturing issues
New Jersey-based Dr Reddy's Laboratories, Inc initiated the Class III recall on November 21 this year. As per USFDA, a Class III recall is initiated in a "situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences".
Aurobindo units recall products in US market for manufacturing issues
The affected lot of the medication, which is used to treat high blood pressure, has been manufactured in India and marketed in the US market by Aurobindo Pharma USA, Inc. As per the USFDA, the company is recalling the affected lot due to "Current good manufacturing practices CGMP deviations: Detection of N-Nitroso-quinapril impurity above the acceptable daily intake limit."
Dr Reddy's, Cipla, Aurobindo units recall products in US market
As per the enforcement report by the US Food and Drug Administration (USFDA), the US-based unit of Dr Reddy's Laboratories is recalling 2,838 ampules of vitamin K deficiency treatment drug Phytonadione Injectable Emulsion. According to the USFDA, Dr Reddy's Laboratories is recalling the affected lot due to "failed stability specifications".
Zydus Lifesciences, Lupin recall products in US market owing to manufacturing issues
Zydus initiated the Class II voluntary recall on July 15 this year. Similarly, Baltimore-based Lupin Pharmaceuticals, Inc, is recalling 7,872 bottles of Rifampin Capsules, a medication used to treat infections caused by bacteria.
Glenmark, Strides Pharma, Cipla recall products in the US
The USFDA noted in its report that the company, a subsidiary of Mumbai-based drug firm, is recalling the affected lot due to "blister package issues." The lot was produced at Glenmark's Pithampur (Madhya Pradesh) based manufacturing facility. The USFDA stated that Glenmark initiated the Class II nationwide (US) recall on June 29 this year.
Thousands of Capri Sun juice packs recalled. Find out why
Approximately 5,760 packs of Capri Sun juice drinks have been recalled by Kraft Heinz due to a possible cleaning solution contamination.
Kia to recall 105,000 Rio cars in Russia
The recall affects Kia Rio models assembled between 2013 and 2018 at the Hyundai Motor Group factory in the Russian city of St Petersburg, Russia's federal agency for technical regulation and metrology (Rosstandard) said.
Okinawa to recall Praise Pro electric scooters after fires
Three of Okinawa's scooters have caught fire since October, resulting in two being injured. Ola Electric, Pure EV and Jitendra EV are other companies that have seen their electric scooters catch fire in the last three weeks.
Sun Pharma, Lupin recall products in US market
According to USFDA, the Mumbai-based drug maker is recalling the affected lot due to "failed moisture limits."
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