RML Medicine Recall: What Patients Need to Know as 10 Critical Drug Batches Fail Quality Checks

Ram Manohar Lohia Hospital has issued an urgent recall for 10 batches of medicines following four separate notices released between Sept 7 and Sept 14
various pills on the table
RML Hospital, Delhi, has issued an urgent recall for 10 batches of medicines soon after they were labelled “Not of Standard Quality”.Ron Lach/pexels
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Dr. Ram Manohar Hospital (RML), Delhi, has issued an urgent recall for 10 batches of medicines soon after they were labelled  “Not of Standard Quality” following four separate notices released between September 7 and September 14.

The oral medications included Sodium Valproate 200 mg, Spironolactone 50 mg, and Imipramine 25 mg, as well as injections of Adenosine, Methyl Ergometrine, Multivitamins, Pheniramine Maleate, and Ascorbic Acid. These medicines are prescribed for various critical treatments, such as, heart conditions, seizure disorders, depression, and postpartum complications.

The administration has ordered all departments and wards to immediately stop the use of these stocks and return them to the assigned drug units. 

What Quality Issues Led to the RML Hospital Medicine Recall?

Of the ten medications, eight were found to be of substandard quality after routine inspections, while tablets of Isosorbide Mononitrate 20 mg and Metoprolol 50 mg were found  in powdered form inside the strips. Both batches were manufactured by Glowsun India Labs Private Limited. 

On September 14, RML’s oral and topical drug unit marked three of the five tablet batches as having failed analytical testing, leading to their recall. Later, five batches of injectable medications also failed analytical testing and were labeled as “Not of Standard Quality” (NSQ). 

How did Previous Quality Control Failure Lead to Seizure of Oxytocin Vials? 

In July 2026, the Delhi Drug Control Department seized and sealed approximately 2,675 vials of Oxytocin from RML Hospital, following sample collection in June. The affected batch was manufactured by Jackson Laboratories Private Limited, Amritsar. Oxytocin is a critical hormone used to induce labor and control excessive bleeding (postpartum hemorrhage) after childbirth. 

Also Read : Rajasthan Bans Oxytocin Amid Probe Into 5 Maternal Deaths in Kota as Tests Find Missing Active Ingredient

What Has RML Hospital Said About the Medicine Recall?

In a report by the Times of India, the hospital administration stated: “The hospital initiated the recall process and issued recall letters for the identified medicines. All relevant units were advised to immediately stop using affected medicines and report any patient-related adverse events, if observed,”. 

Officials added that no adverse reactions or alarming health effects  have been reported by patients in relation to the affected medications. 

“The hospital has made interim arrangements to ensure the availability of alternative medicines and avoid any disruption in patient care. The situation is being closely monitored, and all necessary measures are being taken in accordance with established drug quality and patient-safety protocols,” an RML official told The Times of India.  

What Should Patients and Caregivers Know About the Recalled Drugs? 

According to the official notices, all defective drugs from the affected batches were directed to be returned by clinical departments by September 18, whereas the powdered and substandard tablets were required to be sent back within three days of the respective notice being issued. 

To prevent lapses in patient care, the hospital has arranged alternative medications to ensure that treatment cycles for chronic and acute conditions remain uninterrupted. 

close up shot of pills and syringe
All defective drugs from the affected batches were directed to be returned by clinical departments by September 18.Maksim Goncharenok/pexels

Why are Substandard Drugs Dangerous to Patient Health?

Substandard drugs can have serious consequences for patient health, including treatment failure, accelerated disease progression, antimicrobial resistance, and even fatal outcomes. 

 Poor quality drugs may contain toxic contaminants or incorrect dosage of active ingredients that can prove fatal. 

They can also trigger reactions, such as, rashes, hives, other health risks, that can further increase the overall healthcare cost. 

Also Read : UK Child’s Suspected Brain Tumor Revealed as Vitamin D Toxicity from Defective Supplement Batch

What Should Patients Do If They Have a Recalled Batch? 

  1. Do not discontinue an essential prescription medicine without consulting a healthcare provider. 

  2. Contact your prescribing physician if you suspect that you have a recalled batch.

  3. Seek emergency medical care for serious symptoms, such as difficulty in breathing, swelling, severe allergic reactions, loss of consciousness or seizures. 

Conclusion 

This incident has raised questions about why the hospital’s drug quality surveillance framework is not being strengthened. 

It is critical to identify defects at the batch level before the medication is prescribed to patients. 

Quality control protocols must be significantly more rigorous, especially, for life-saving and crucial therapies. 

(Rh/APC/MSM)

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