# FDA recall D-1129-2017

> **Degasa Sa De Cv** · Class II · drug recall initiated 2017-08-04.

## Product

Povidone Iodine, USP Prep Solution, 10%, packaged in 1 gallon bottle, OTC, Manufactured for PSS World Medical, Inc. Southpoint Blvd. Jacksonville, FL  Made in Mexico, NDC 68345-350-09

## Reason for recall

Labeling: Label mix-up. Finished product Povidone iodine 7.5% was labeled as Povidone iodine 10% , the outer box had the correct label.

## Distribution

CA, IL.

## Key facts

- **Recall number:** D-1129-2017
- **Recalling firm:** Degasa Sa De Cv
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-08-04
- **Report date:** 2017-09-13
- **Termination date:** 2020-11-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Jiutepec, N/A, Mexico

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1129-2017

## Citation

> AI Analytics. FDA recall D-1129-2017. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-1129-2017. Source: US FDA. Licensed CC0.

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