FDA recall,
Parnell Sevoflurane Inhalation Anesthetic for Dogs
Sevoflurane inhalation solution has a bottle collar notch pattern incompatible with the sevoflurane-specific anti-spill pour spout.
Summary by Recall Canary from the FDA notice
What happened
Parnell Techologies Pty, LTD. is recalling Sevoflurane, 250 mL, Nonflammable, Nonexplosive, Inhalation Anesthetic, For Use in Dogs, Distributed by: Parnell US 1. Inc., because the yellow collar notch pattern on the bottle is incompatible with the yellow sevoflurane-specific anti-spill pour spout notch pattern. The recall began July 17, 2026, and was added to the FDA's Enforcement Report on July 31, 2026. The product was distributed nationwide.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medicine recalls:
- Check the FDA or company notice for instructions specific to this product.
- Ask your pharmacist or doctor whether your lot is affected and what to do.
Is yours affected?
Match the NDC and batch code listed under your product.
An NDC (National Drug Code) is usually printed on the drug's label.
Sevoflurane, 250 mL, Nonflammable, Nonexplosive, Inhalation Anesthetic, For Use in Dogs
- NDC
- 68504-011-01
- Batch code
- 5122509001A
Recall details
- Company began the recall
- Sold in
- Nationwide
- Company
- Parnell Techologies Pty, LTD.
- Event ID
- 99477
- Quantity recalled
- 4,440 units
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
