EMD Millipore Corporation recalls Lugol s Iodine Solution 500ML, Part Number 624-71
Due to the incorrect packaging utilized with lot 3124, there' s an improper seal between the cap and bottle. With an improper seal the Assay (current specification of 24.8 to 27.2 mL) is expected to continue to drop…
Read the official notice →- Date
- 2023-12-06
- Country
- United States
- Brand
- EMD Millipore
- Product
- Lugol s Iodine Solution 500ML, Part Number 624-71
- Classification
- Class II
- Units
- US States: CA, NJ, WV
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More EMD Millipore recalls
- 2024-03-06
USEMD Millipore Corporation recalls Schiff Reagent, Hotchkiss-McManus, packaged in an amber glass bottle with a black polypropylene cap.
This IVD is colorless. A customer complaint was received noting it appeared pink. A review of inventory confirmed additional stock appeared pink.
FDA · DeviceEMD Millipore CorporationDomestic: AL, IL, MA, MN, NJ, PA, TX, VA. Foreign: Canada.Official notice →
Other drugs & medical recalls in the United States
- 2023-12-06
- US
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- US
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There is the potential for the needle drive to become dislodged and/or broken which could result in uncontrollable movement.
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Produced with unintended open slits on the side of the mouthpiece body, may result in insufficient ventilation in spontaneous breathing patients using MPV-VCV and MPV-PCV modes of ventilation