oAlert.pl
WARNING: RECALLED PRODUCT
PL EN

Metronidazole B. Braun

Cross-contamination of infusion solutions in the listed batches of B. Braun medicinal products was detected. Potential effects: poisoning, severe adverse reactions, lack of therapeutic efficacy.

Download the app and stay informed

Get instant notifications about recalled products and protect your family.

App Store Google Play
Metronidazole B. Braun
Risk Level
Critical
Manufacturer
B. Braun Melsungen AG, Carl-Braun-Straße 1, 34212 Melsungen, Niemcy
Batch Number
21027402
EAN Code
05909990715190
Recall Date
04.08.2023
Category
Medicines & supplements
View official statement

Important Information

What You Should Know

Recommendations

Do not use products from the listed batches. Check the batch number of any bottles held; if affected, return the product to a pharmacy or healthcare provider. If a product from a withdrawn batch has b...

Actions Taken

The Chief Pharmaceutical Inspector withdrew the specified batches of B. Braun infusion solutions from the entire Polish market and granted the decision immediate enforceability after receiving a Rapid...

Need Help?

If you feel unwell after consuming this product, contact your doctor or call the poison control center.

FAQ

Frequently Asked Questions

Is this product safe to consume?
No. This product has been recalled due to: Cross-contamination of infusion solutions in the listed batches of B. Braun medicinal products was detected. Potential effects: poisoning, severe adverse reactions, lack of therapeutic efficacy.
What should I do if I already bought this?
Stop using the product immediately. Return it to the store for a full refund. If you consumed it and feel unwell, contact your doctor.
Which batches are affected?
Affected batch numbers: 21027402

Related

Other Recalled Products

Lorafen

Lorafen

06.02.2026
Carmustine Accord

Carmustine Accord

03.02.2026
Taromentin

Taromentin

30.01.2026
Plerixafor MSN

Plerixafor MSN

29.01.2026
Zoledronic Acid Noridem

Zoledronic Acid Noridem

29.01.2026