Methylphenidate Hydrochloride Tablets, USP 20mg, Rx Only, 100 Tablets per bottle, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901, Distributed by: Sun Pharmaceutical Industries Inc., Cranbury, NJ 08512, NDC 57664-230-88.
Reported: August 2, 2023 Initiated: July 13, 2023 #D-0940-2023
Product Description
Methylphenidate Hydrochloride Tablets, USP 20mg, Rx Only, 100 Tablets per bottle, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901, Distributed by: Sun Pharmaceutical Industries Inc., Cranbury, NJ 08512, NDC 57664-230-88.
Reason for Recall
Presence of Foreign Substance: Metal embedded in a tablet.
Details
- Recalling Firm
- SUN PHARMACEUTICAL INDUSTRIES INC
- Units Affected
- 7313 bottles
- Distribution
- Nationwide
- Location
- Princeton, NJ
Frequently Asked Questions
What product was recalled? ▼
Methylphenidate Hydrochloride Tablets, USP 20mg, Rx Only, 100 Tablets per bottle, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901, Distributed by: Sun Pharmaceutical Industries Inc., Cranbury, NJ 08512, NDC 57664-230-88.. Recalled by SUN PHARMACEUTICAL INDUSTRIES INC. Units affected: 7313 bottles.
Why was this product recalled? ▼
Presence of Foreign Substance: Metal embedded in a tablet.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 2, 2023. Severity: Moderate. Recall number: D-0940-2023.
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