Ruzurgi Amifampridine 10 mg Tablet Bottle
AustraliaRuzurgi Amifampridine 10 mg Tablet Bottle
Grund für den Rückruf / Gefahr
TranslatedThe affected product batch 18039 exceeds the specification for total yeast and mould counts (TYMC).
Produktbeschreibung & Identifikation
TranslatedReason / Defects: The affected product batch 18039 exceeds the specification for total yeast and mould counts (TYMC). Hazards: The effects of increased exposure to yeast and/or mould can include allergic reactions, asthma, neurotoxicity, sinusitis, otomycosis, onychomycosis, keratitis, respiratory infections, skin infections, and systemic infections. This may pose a serious health risk to users with weakened immune systems. What to do: Consumers who have been prescribed Ruzurgi Amifampridine 10 mg tablets, should check the batch number printed on the bottle. This recall does not affect any other batch of Ruzurgi, or any other ORSPEC Pharma products. Consumers will be contacted by a clinician to arrange for a replacement product. Anyone who is concerned about the use of this batch of product should consult their doctor. For more information, consumers can contact ORSPEC Pharma Customer Service on 02 4339 4239.
Betroffene Produkte
TranslatedRuzurgi amifampridine 10 mg tablet bottle Batch Number: 18039 Exp: 3/2023 Supplied via Special Access Scheme (SAS)
Additional Source Details
| Field | Value |
|---|---|
| Guid › #text | 8b2e0847-f8a3-41fb-a887-5d9ae96b1f67 |
| Guid › @ is Perma Link | false |
| Link | https://www.productsafety.gov.au/search-consumer-product-recalls/ruzurgi-amifampridine-10-mg-tablet-bottle |
| Pub Date | Mon, 04 Oct 2021 00:00:00 +0000 |
Consumer Action Protocol: What You Should Do Immediately
Safety StepsCheck the model number, serial number, and date stamp on the rating label on the back or underside of the product.
Immediately discontinue using the product. Unplug electrical items and keep juvenile items out of reach of children.
Under statutory consumer protection rules, consumers are entitled to a full refund, certified replacement, or free repair kit without needing the original sales receipt.
If you suffered an injury, illness, or property damage from this product, file an official incident report with regulatory authorities (Australia Products).
Your Legal Rights as a Consumer
Recalls are legally binding corrective safety actions overseen by statutory government bodies. Recalling entities are legally prohibited from charging consumers for official safety remedies. If a retailer or dealership refuses your recall remedy, notify the issuing regulatory agency immediately.
Frequently Asked Questions About This Recall
FAQ GuideQ1:What should I do immediately if I own or bought Ruzurgi Amifampridine 10 mg Tablet Bottle?
Immediately stop using the product and keep it out of reach of children. Disconnect power if electrical, and do not attempt makeshift home repairs.
Q2:Can I get a full refund or free repair for this recall?
Yes. Recalling manufacturers and retail merchants are required under consumer protection regulations to offer a statutory remedy—typically a full refund, certified repair kit, or replacement unit.
Q3:Do I need my original sales receipt to claim a remedy or refund?
In most recall cases, no receipt is required. Because safety recalls are matters of public health and statutory compliance, retailers and manufacturers routinely issue refunds, store credit, or replacement kits upon presentation of the affected product or lot code.
Q4:Where can I verify official information for this safety alert?
This safety alert is aggregated directly from official regulatory agency records (Australia Products). You can click the 'Official Agency Alert' link on this page to view the primary government notice and contact the manufacturer directly.
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🚨 SAFETY ALERT: Ruzurgi Amifampridine 10 mg Tablet Bottle Check if your household is affected: https://therecallfile.com/de/recalls/ruzurgi-amifampridine-10-mg-tablet-bottle/AU-8b2e0847-f8a3-41fb-a887-5d9ae96b1f67
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