Zimmer Spine, Inc. is initiating a voluntary worldwide recall of all 315 units of the PEEK Ardis® Inserter. The Ardis Inserter is a surgical instrument used during spinal surgery to implant the PEEK Ardis Interbody Spacer. The inserters are being recalled because Zimmer Spine has received reports of PEEK Ardis Interbody Spacer implant breakage when … [Read more...]
Mobius Therapeutics, LLC Issues a Voluntary Recall of Mitosol® (mitomycin forsolution), 0.2 mg/vial, Kit for Ophthalmic Use
Mobius Therapeutics, LLC, St. Louis, MO, announced today that it is conducting a voluntary recall of 2 lots of Mitosol® (mitomycin for solution), 0.2 mg/vial, Kit for Ophthalmic Use. The company is taking this voluntary action due to the fact that we cannot exclude the possibility that the affected lots may be non-sterile. These two lots of Mitosol … [Read more...]
Advance Pharmaceutical Rcalls One Lot (# 12G468) of Ferrous Sulfate Tablets, 325 mg, that may actually contain Meclizine HCl 25 mg tablets
Advance Pharmaceutical Inc. today announced that it is conducting a voluntary nationwide recall of one lot of Ferrous Sulfate Tablets, 325 mg, Lot 12G468 Exp. 07/14, UPC Barcode 0 0536-5890-01 3. The lot was manufactured and packaged in 100 count bottles by Advance Pharmaceutical Inc. under the label of Rugby NATURAL IRON SUPPLEMENT Ferrous … [Read more...]
Voluntary Worldwide Field Corrective Action Issued for the T-piece Circuit used on GE Healthcare’s Giraffe and Panda
GE Healthcare initiated a voluntary worldwide field correction of the T-piece circuit used with GE Healthcare's Giraffe and Panda resuscitation units. The T-piece circuits affected by this recall are sold under the following part numbers and contain a red inspection stamp (those containing a blue inspections stamp are NOT affected by this … [Read more...]
ADM Alliance Nutrition Recalling MoorMan’s® ShowTec® 18 Elite Lamb Feed
ADM Alliance Nutrition, Inc. ("Alliance Nutrition") is recalling 50-pound bags of MoorMan's® ShowTec® 18 Elite Lamb DC, product number 80939MPS, because the product has high levels of copper. There are three lot numbers involved in this recall: BF23512, BF27812, and BF29312. These were distributed between Aug. 24, 2012, and Nov. 21, 2012. The … [Read more...]
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