Published by Reclia Safety Desk | July 17, 2026
📌 EU Safety Gate Recall Notice
Product: Rodenticide
Brand: Rodentin
Country: Germany
Hazards: Chemical Risk, Non-Compliance
What to do: Stop using this product. Follow the recall instructions for refund or replacement.
Case #SR/02020/26 |
View original notice →
Recall Summary
| Product | Rodenticide |
| Brand | Rodentin |
| Country | Germany |
| Case Number | SR/02020/26 |
| Hazard | Chemical Risk, Non-Compliance |
| Source | 🇪🇺 EU Safety Gate |
Recall Information Record – Reclia Database
1. Recall Summary
This recall notice, case number SR/02020/26, was issued by the notifying country Germany and published on the EU Safety Gate system. The recall involves a rodenticide product sold under the brand name Rodentin. The specific product name is “FORTE – Power bait blocks.” The product is described as a concentrated rodenticide in the shape of blocks intended for use against rodents. The product type is listed as “Professional,” indicating it is intended for professional use rather than general consumer sale. The country of origin is listed as Unknown. The recall was initiated due to the product not being authorized for sale to the general public and due to non-compliance with EU regulations.
2. Affected Products
– Product: Rodenticide
– Brand: Rodentin
– Name: FORTE – Power bait blocks
– Type/Model Number: Not specified in the recall notice.
– Batch Number: Not specified in the recall notice.
– Barcode: Not specified in the recall notice.
– Production Dates: Not specified in the recall notice.
– Country of Origin: Unknown
– Notifying Country: Germany
– Case Number: SR/02020/26
3. Hazard Information
The recall notice identifies the risk type as “Chemical” and the level as “Serious risk.” The specific danger stated in the source data is as follows: The product has not been authorised for sale to the general public. The product has an excessive concentration of bromadiolone (measured value: 0.05 g/kg by weight). Bromadiolone can cause inhibition of blood clotting, damage to blood vessels leading to internal bleeding, and organ damage in case of ingestion. The product does not comply with the Biocidal Products Regulation nor with the REACH Regulation.
4. Consumer Action Required
The recall notice does not provide specific instructions directed at consumers regarding what they should do if they possess this product. The measures listed in the source data are directed at economic operators (distributors). Consumers who have purchased or are in possession of this product should refer to the official remedy and contact information below. No recall URL or specific consumer hotline is provided in the source data.
5. Official Remedy
The official measures ordered by the notifying country (Germany) are as follows, as stated in the source data:
– Type of economic operator to whom the measure(s) were ordered: Distributor
– Category of measure(s): Ban on the marketing of the product and any accompanying measures
– Date of entry into force: 02/12/2025
– Type of economic operator taking notified measure(s): Distributor
– Category of measure(s): Stop of sales
– Date of entry into force: 15/02/2026
These measures indicate that the distributor was ordered to ban the marketing of the product and to stop sales. No specific remedy for consumers (such as refund, replacement, or disposal instructions) is detailed in the source data.
6. Contact Information
– Notifying Country: Germany
– EU Safety Gate Reference: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10099414
– Case Number: SR/02020/26
– Company Recall Code: Not specified in the recall notice.
– URL for Recall: Not specified in the recall notice.
Consumers seeking further information or wishing to report a product issue may contact the relevant national consumer safety authority in Germany or consult the EU Safety Gate website using the reference link provided. No direct phone number or email address for the manufacturer or distributor is included in the source data.
Recall Timeline
- **Current** – Recall announced via EU Safety Gate
- **Ongoing** – Consumers advised to stop using product
- **Ongoing** – Refund or replacement available from manufacturer
Frequently Asked Questions
Q: How do I identify the recalled Rodenticide?
A: Check the product label and packaging against the official EU Safety Gate recall notice (Case #SR/02020/26).
Q: What should I do if I own the recalled Rodenticide?
A: The recall notice advises consumers to stop using the product immediately and follow the recall instructions.
Q: How do I get a refund or replacement for the recalled Rodenticide?
A: Contact the manufacturer or retailer using the information in the recall notice.
Q: What are the health risks from this chemical hazard?
A: The recall notice identifies specific chemicals of concern. Contact a healthcare provider if you have health concerns.
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Disclaimer: Information on this page is summarized from official EU Safety Gate recall notices.
Reclia is a recall information database and does not conduct product testing, safety certification,
or independent investigations.
Consumers should refer to the original EU Safety Gate notice
for complete details and official instructions.