Bicillin L-A 600000 Units/mL Inj., Qty: 20 mL Syringe, MFG by: King Pharma Inc., Bristol, TN 37620, Repackaged by: RemedyRepack, Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 61786-0253-03
Reported: December 16, 2015 Initiated: November 11, 2015 #D-0512-2016
Product Description
Bicillin L-A 600000 Units/mL Inj., Qty: 20 mL Syringe, MFG by: King Pharma Inc., Bristol, TN 37620, Repackaged by: RemedyRepack, Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 61786-0253-03
Reason for Recall
Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.
Details
- Recalling Firm
- RemedyRepack Inc.
- Units Affected
- 60 Vials
- Distribution
- Nationwide
- Location
- Indiana, PA
Frequently Asked Questions
What product was recalled? ▼
Bicillin L-A 600000 Units/mL Inj., Qty: 20 mL Syringe, MFG by: King Pharma Inc., Bristol, TN 37620, Repackaged by: RemedyRepack, Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 61786-0253-03. Recalled by RemedyRepack Inc.. Units affected: 60 Vials.
Why was this product recalled? ▼
Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on December 16, 2015. Severity: Moderate. Recall number: D-0512-2016.
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