Solutions Rx Recalls C-Budesonide Capsules Due to Penicillin Risk
Solutions Rx Pharmacy recalls c-Budesonide 0.6MG capsules due to possible penicillin cross-contamination. Check lot numbers and expiration dates for affected batches.
Use caution until it’s fixed
Penicillin Cross Contamination - Possible presence of penicillin in bulk budesonide powder used to compound prescription nasal rinse/nebulizer capsules.
Contact the company
What happened, in plain English
Solutions Rx Pharmacy is recalling c-Budesonide 0.6MG capsules because the bulk powder used may be contaminated with penicillin. This contamination poses a risk of allergic reaction for individuals sensitive to penicillin. The recall covers specific lots distributed in Alabama, Georgia, Tennessee, and Louisiana. Read more at govinfonow.com/recall/44149-solutions-rx-pharmacy-recalls-c-budesonide-0-6mg-capsules-60.
Source Summary by GovInfoNow · govinfonow.com/recall/44149-solutions-rx-pharmacy-recalls-c-budesonide-0-6mg-capsules-60 · Updated October 12, 2026 · FDA enforcement record: FDA #D-0385-2016
Cite this page
“Solutions Rx Recalls C-Budesonide Capsules Due to Penicillin Risk.” GovInfoNow, updated October 12, 2026. https://govinfonow.com/recall/44149-solutions-rx-pharmacy-recalls-c-budesonide-0-6mg-capsules-60. Based on FDA recall #D-0385-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0385-2016%22&limit=1).
Why it’s dangerous
The hazard is the possible presence of penicillin in the bulk budesonide powder used to compound the capsules. If a person with a penicillin allergy uses these contaminated capsules, they could experience an allergic reaction.
Who’s affected
Patients who have been prescribed c-Budesonide capsules for nasal rinses or nebulizers by Solutions Rx Pharmacy. Individuals with known penicillin allergies are at the highest risk of an adverse reaction.
How to tell if you have this one
Look for c-Budesonide 0.6MG capsules in a 60-count bottle labeled 'NOT FOR ORAL USE-USE IN NASAL RINSE OR NEBULIZER'. Affected lots include 04-24-2015-D (Exp 05/31/15) and multiple lots with expiration date 06/16/15, such as 03-13-2015-C through 06/10-2015-J.
- Brand
Solutions Rx Pharmacy- Category
Drug
What to do — step by step
Check Your Lot Numbers
Compare the lot numbers on your bottle against the recalled lots listed in the record, such as 04-24-2015-D or any lot expiring 06/16/15.
Stop Using Affected Capsules
If you have the recalled product, discontinue use immediately to avoid potential penicillin exposure.
Contact Your Pharmacy
Reach out to Solutions Rx Pharmacy or your healthcare provider for instructions on replacement or disposal.
Where it went and when
Where it was distributed
Distributed in 4 states.
FDA distribution: “AL, GA, TN, LA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Georgia, Louisiana, Tennessee.
Recall timeline
FDA terminated this recall 5 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
Which lot numbers are affected?
Affected lots include 04-24-2015-D (Exp 05/31/15) and several others expiring 06/16/15, including 03-13-2015-C, 03-18-2015-F, 03-18-2015-G, 03-23-2015-C, 03-24-2015-C, 04-02-2015-G, 04-14-2015-F, 04-14-2015-G, 04-22-2015, 05-06-2015-B, 05-14-2015-D, 05-22-2015-F, 05-27-2015-C, 06-02-2015-E, and 06/10-2015-J.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0385-2016 (June 22, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0385-2016 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 12, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.