Safe Tussin DM Cough + Chest Congestion (Dextromethorphan HBr/ Cough Suppressant Guaifenesin/Expectorant), packaged in 4.0 FL OZ(118mL), 2020 Kramer Laboratories, Inc. Bridgewater, NJ 08807
Reported: August 2, 2023 Initiated: June 23, 2023 #D-0942-2023
Product Description
Safe Tussin DM Cough + Chest Congestion (Dextromethorphan HBr/ Cough Suppressant Guaifenesin/Expectorant), packaged in 4.0 FL OZ(118mL), 2020 Kramer Laboratories, Inc. Bridgewater, NJ 08807
Reason for Recall
CGMP Deviations: use of non-food grade lubricant in mixing vessel.
Details
- Recalling Firm
- Kramer Laboratories, Inc.
- Units Affected
- N/A
- Distribution
- nationwide within the United States
- Location
- Bridgewater, NJ
Frequently Asked Questions
What product was recalled? ▼
Safe Tussin DM Cough + Chest Congestion (Dextromethorphan HBr/ Cough Suppressant Guaifenesin/Expectorant), packaged in 4.0 FL OZ(118mL), 2020 Kramer Laboratories, Inc. Bridgewater, NJ 08807. Recalled by Kramer Laboratories, Inc.. Units affected: N/A.
Why was this product recalled? ▼
CGMP Deviations: use of non-food grade lubricant in mixing vessel.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 2, 2023. Severity: Moderate. Recall number: D-0942-2023.
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