Class II · Moderate risk
Lipo-C (Methionine 25 mg/Inositol 50 mg/Choline Chloride 50 mg/Carnitine (L)
Lack of Assurance of Sterility
Is Dexpanthenol recalled?
Yes — there is an active recall. 11 ongoing FDA recalls mention Dexpanthenol (43 total). Check the affected lots below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Dexpanthenol. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Dexpanthenol recalls on record
none so far in 2026; 43 on record, newest first
Class II · Moderate risk
IV Cocktail #2
Lack of Assurance of Sterility
Class II · Moderate risk
Infuvite IV
Lack of Assurance of Sterility
Class II · Moderate risk
Dexpanthenol 250 mg/mL
Lack of Assurance of Sterility
Class II · Moderate risk
Dexpanthenol 250mg/Ml W/Pres.
Lack of Assurance of Sterility
Class II · Moderate risk
Dexpanthenol 250mg/Ml
Lack of Assurance of Sterility
Class II · Moderate risk
Dexpanthenol Injection
Lack of Assurance of Sterility
Class II · Moderate risk
Dexpanthenol
Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Class II · Moderate risk
Dexpanthenol 250 mg/ml Injectable
Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility
Class II · Moderate risk
Dexpanthenol 215 mg/ml Injectable
Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility
Class II · Moderate risk
DEXPANTHENOL with preservative
Lack of Sterility Assurance: All lots of sterile products compounded by the pharmacy that are not expired due to concerns associated with quality control procedures that present a potential risk to sterility assurance that were observed during a recent FDA inspection.
Class II · Moderate risk
Dexpanthenol 250 mg/mL PF
Lack of Assurance of Sterility: The product lots are being recalled due to laboratory results indicating microbial contamination. The FDA was concerned test results obtained from the recalling firm's contract testing lab may not be reliable.
Class II · Moderate risk
Dexpanthenol 250mg/ml PF
The product lots are being recalled due to laboratory results indicating microbial contamination. The FDA was concerned test results obtained from the recalling firm's contract testing lab may not be reliable.
Class II · Moderate risk
Dexpanthenol 250 Mg/Ml Injectable
Lack of Assurance of Sterility; FDA inspectional findings resulted in concerns associated with quality control procedures that impacted sterility assurance
Class II · Moderate risk
Dexpanthenol 250 mg/ml Injection
Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
Class II · Moderate risk
Dexpanthenol 200 mg/mL Injectable
Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
Class II · Moderate risk
Dexpanthenol Injection
Lack of Assurance of Sterility: all sterile products compounded, repackaged, and distributed by this compounding pharmacy due to lack of sterility assurance and concerns associated with the quality control processes.
Class II · Moderate risk
Dexpanthenol 250mg/Ml Injectable 100 Ml
Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all Sterile Human Drugs distributed between 11/21/2011 and 05/21/2012 because FDA environmental sampling revealed the presence of microorganisms and fungal growth in the clean room where sterile products were prepared.
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