Reported Feb 6, 2013 · Terminated
Hydrocodone bitartrate and acetaminophen Tablets, USP, 10 mg/500 mg, packaged in a) 30-count bottles, NDC 0603-3888-16;…
Vintage Pharmaceuticals LLC dba Qualitest Pharmaceuticals
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals · 120 Vintage Dr NE · Huntsville, AL · 35811-8216
Is this the product you have?
9 of 9 products
| # | Product as published |
|---|---|
| 1 | 30-count bottles, NDC 0603-3888-16 |
| 2 | 60-count bottles, NDC 0603-3888-20 |
| 3 | 90-count bottles, NDC 0603-3888-02 |
| 4 | 100-count bottles, NDC 0603-3888-21 |
| 5 | 120-count bottles, NDC 0603-3888-22 |
| 6 | 150-count bottles, NDC 0603-3888-26 |
| 7 | 180-count bottles, NDC 0603-3888-04 |
| 8 | 500-count bottles, NDC 0603-3888-28; and |
| 9 | 1000-count bottles, NDC 0603-3888-32, Rx only, Mfg. for: Qualitest Pharmaceuticals, Huntsville, AL 35811. |
- Lot codes and dates
9 of 9 products
Products covered by this recall # Product as published 1 C1160712C, Exp 12/13 2 C0930812A, C1110412A, C1141012B, C1160712A, Exp 12/13 3 C0950812B, C1110412B, C1151012B, C1160712B, C1530512A, Exp 12/13 4 C0540212A, C0550212A, C0560212A, C0710312A, C0720312A, C0730112B, C0730312A, C0740112B, C0740312A, C0750112A, C0760112A, C0770112C, C0780112C, C0790112C, C0860812A, C0870812A, C0880812A, C0890812A, C0900812A, C0910812A, C0920812A, C0950412A, C0950812D, C0960412A, C0970412A, C0980412A, C1030412A, C1040412A, C1050412A, C1060412A, C1061012A, C1070412A, C1071012A, C1081012A, C1101012A, C1111012A, C1120412A, C1121012A, C1130412A, C1131012A, C1140412A, C1141012A, C1160712D, C1440512A, C1450512A, C1460512A, C1470512A, C1510512A, C1520512A, C1530512B, C1540512A, C1550512A, C1560512A, C1570512A, Exp 12/13 5 C0670312A, C0680312A, C0930812B, C0950812C, Exp 12/13 6 C1160712E, Exp 12/13 7 C0950812A, C1110412C, Exp 12/13 8 C0630212B, C0640212B, C0690312A, C0700312A, C0720112B,C0940812A, C0941112A, C0960812A, C1010412B, C1020412B, C1080412A, C1090412A, C1100412A, C1170712A, C1180712A, C1480512A, C1490512A, C1500512A, Exp 12/13 9 C0570212B, C0580212B, C0590212B, C0600212A, C0610212A, C0620212A, C0750312A, C0760312A, C0930812C, C0970812A, C0990412A, C1000412A, Exp 12/13 - Amount recalled
- 897,379 bottles
Where it was sold
- Nationwide
- PR
Why it was recalled
Stop using this product now
Superpotent (Multiple Ingredient) Drug: Complaint received of oversized tablets.
Using this product could cause serious injury, illness or death — stop using it now.
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