Safety Alerts & Recalls
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Latest Alerts
Paddock Laboratories, Inc. Recalls Single Lot of Moexipril Tablets 7.5mg
Paddock Laboratories, Inc.has recalled a single lot of Moexipril Tablets 7.5mg. Lot number 2012028142 has been recalled because this lot failed the manufacturer’s routine test that measures the tablets’ ability to dissolve.
Moexipril is used in the treatment of high blood pressure. Moexipril is also sold under the brand name Univasc. No other lots, strengths, or brands of Moexipril were involved in this recall.
To view the FDA notice about this recall, please visit:
http://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Event-Detail.cfm?action=detail&id=63354&w=10172012&lang=eng
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Sandoz Inc. Recalls Several Lots of Children's Cetirizine Chewable Tablets 5 mg
Sandoz Inc. is recalling several lots of Children's Cetirizine Chewable Tablets 5 mg. The following lot numbers are being recalled because samples from this lot did not pass the manufacturer's routine tests for impurities and by-products from chemical breakdown over time: BT2862, BT7986, BT7994, BW0652, CC1961, CA3437, and BW0665.
Children's Cetirizine contains the active ingredient Cetirizine and is commonly used in the treatment of allergies. Cetirizine is also sold under the brand name Zyrtec. This recall alert only applies to the select lots of Children's Cetirizine HCl Chewable Tablets 5 mg. No other Cetirizine products were involved in this recall.
To view the FDA notice about this recall, please visit:
http://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Event-Detail.cfm?action=detail&id=63224&w=10242012&lang=eng
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