Lisinopril Recall in France: Check Your Medication
Lisinopril Recall: Over 32,000 Boxes Pulled in France Due to Printing Error
Table of Contents
- Lisinopril Recall: Over 32,000 Boxes Pulled in France Due to Printing Error
- Lisinopril Recall in France: Your Questions Answered
- What is the Lisinopril Recall About?
- Why Was Lisinopril Recalled in France?
- What Specific Lisinopril Products are Affected?
- what Should I Do If I Have Lisinopril from an Affected Lot?
- what are the Potential Risks of a Lisinopril Overdose?
- Can You Summarize the Key Information About the Lisinopril Recall?
- will New, Compliant, Lisinopril Be Available?
- Where Can I get More Information About This Lisinopril Recall?
PARIS (AP) — French authorities have recalled more than 32,000 boxes of lisinopril, a common medication used to treat hypertension and heart failure. Teh National Medicines Safety agency (ANSM) announced the recall on May 6, citing a printing defect on the packaging as the reason.
reason for the Lisinopril Recall
While the quality of the lisinopril tablets themselves is not in question, the ANSM stated that a ”printing defect” on the blister packs could “induce a risk of overdose.” The agency elaborated, explaining that “the inscription present on the aluminum of the brochure can lend itself to confusion because it suggests that it is necessary to take several tablets on certain days.” This ambiguity could lead patients to take incorrect dosages.
Affected Lisinopril Lots
The recall affects four specific lots of Lisinopril 5 mg manufactured by Viatris:
- Box of 28 tablets: Lot 8172295, expiration date 01/2026
- Box of 28 tablets: Lot 8189879, expiration date 03/2027
- Box of 84 tablets: Lot 8172296, expiration date 01/2026
- Box of 84 tablets: Lot 8192737, expiration date 03/2027
the ANSM clarified that the 20 mg dosage of lisinopril is not affected by this particular printing error.
What to Do If You Have Affected Medication
The ANSM advises patients not to interrupt their lisinopril treatment. Instead, individuals who possess boxes from the affected lots should return them to their pharmacy. Pharmacists will exchange the recalled boxes for compliant ones, potentially from a different manufacturer than Viatris. The agency anticipates that new, compliant lots of lisinopril will be available soon.
Potential Risks of Overdose
According to the ANSM, potential side effects of lisinopril overdose include fatigue, balance disorders, and hypotension (low blood pressure). In some cases, an alteration of renal function may also occur. These side effects might potentially be more pronounced in individuals with pre-existing kidney failure. The agency urges anyone experiencing adverse effects to contact their doctor promptly.
Lisinopril Recall in France: Your Questions Answered
What is the Lisinopril Recall About?
French authorities have recalled over 32,000 boxes of lisinopril due to a printing error on the packaging, as announced by the National Medicines Safety agency (ANSM). Lisinopril is a common medication used to treat high blood pressure (hypertension) and heart failure.
Why Was Lisinopril Recalled in France?
The recall was initiated because of a printing defect on the blister packs. This defect could cause confusion about the correct dosage, perhaps leading patients to take an incorrect amount of the medication and consequently, a possible overdose. The ANSM explicitly stated that the quality of the lisinopril tablets themselves is not in question.
What Specific Lisinopril Products are Affected?
The recall affects specific lots of Lisinopril 5 mg manufactured by Viatris. The 20 mg dosage is not currently affected. Here are the specific lots:
- box of 28 tablets: Lot 8172295, expiration date 01/2026
- Box of 28 tablets: Lot 8189879, expiration date 03/2027
- Box of 84 tablets: Lot 8172296, expiration date 01/2026
- Box of 84 tablets: Lot 8192737, expiration date 03/2027
what Should I Do If I Have Lisinopril from an Affected Lot?
The ANSM advises patients not to stop their lisinopril treatment. You should take your affected medication to your pharmacy. The pharmacist will then exchange the recalled boxes for compliant ones. These boxes may be from a different manufacturer than Viatris.
what are the Potential Risks of a Lisinopril Overdose?
Potential side effects of a lisinopril overdose include:
- Fatigue
- Balance disorders
- Hypotension (low blood pressure)
- Possible alteration of renal function
These side effects could be more severe in individuals with pre-existing kidney problems. The ANSM urges anyone experiencing adverse effects to seek prompt medical advice.
Can You Summarize the Key Information About the Lisinopril Recall?
Here’s a quick summary:
| Aspect | Details |
|---|---|
| Medication | Lisinopril 5mg (Viatris) |
| Reason for Recall | Printing defect causing potential dosage confusion |
| Affected Lots | See the list under ”Affected Lisinopril Lots” |
| Action Required | Return affected boxes to the pharmacy for exchange |
| Do Not | Stop your treatment |
will New, Compliant, Lisinopril Be Available?
Yes, the ANSM anticipates that new, compliant lots of lisinopril will be available soon.
Where Can I get More Information About This Lisinopril Recall?
The original article dose not contain information for additional sources. Contact your pharmacist or medical professional for specific questions. Be prepared to provide the lot number of your medication.