State
73,827 recalls have nationwide distribution and so reach South Carolina. 7,153 additional recalls listed South Carolina specifically in their distribution scope.
Of the 7,153 recalls naming South Carolina we have scored against our rubric, 1,275 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,170 (30%) are Severe.
Which agencies issued them
These figures cover only the 7,153 recalls whose distribution notice names South Carolina specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Kellogg Company is voluntarily recalling Keebler Animal Totes due to a potential undeclared peanut allergen resulting from a supplier's flour recall.
PharMEDium Services is recalling 4,081 bags of 0.1% Bupivacaine HCl injectable solution because the active ingredient was contaminated with glass particulate matter.
WalkMed Infusion is voluntarily recalling Triton Administration Sets because they may contain particulate matter. The recall affects 383 cases distributed nationwide.
WalkMed Infusion is voluntarily recalling specific lots of IV administration sets due to the potential presence of particulate matter on or in the devices.
Parker Medical is voluntarily recalling Trach-Vac Endotracheal Tubes because they may kink during use, potentially affecting patient ventilation.
Kellogg Company is voluntarily recalling Keebler 5 Flavor Mod snack items because they may contain undeclared peanut. The recall stems from a supplier's recall of flour.
WalkMed Infusion is voluntarily recalling specific lots of IV administration sets due to the potential presence of particulate matter in or on the devices.
Kellogg Company is voluntarily recalling Special K Mini Brownies Blondie due to potential undeclared peanut from a flour supplier issue.
Smith & Nephew is recalling 563 TWINFIX QUICK-T Knot Pusher Suture Cutters because the sterile packaging may be breached.
WalkMed Infusion is voluntarily recalling specific lots of Triton IV administration sets due to the potential presence of particulate matter in or on the devices.
Kellogg Company is voluntarily recalling Special K Mini Brownies Fudge due to the potential for undeclared peanut allergen from a supplier's flour recall.
Kellogg Company is voluntarily recalling Premium Whole Chocolate Cremes 25 lb because of the potential for undeclared peanut allergen.
WalkMed Infusion is voluntarily recalling specific lots of T100-000VF IV sets due to the potential presence of particulate matter in or on the devices.
Novel Laboratories is recalling Zolpidem Tartrate sublingual tablets because the packaging fails to meet child-resistant closure requirements, posing a risk of poisoning to children.
Kellogg Company is voluntarily recalling Keebler Grahams Crackers Honey in 200-count and 30-count cases because of potential undeclared peanut.
WalkMed Infusion, LLC is voluntarily recalling specific lots of 90-inch IV administration sets due to the potential presence of particulate matter in or on the devices.
Kellogg Company is voluntarily recalling Mother's Double Chocolate Chip Minis Cookies due to a potential undeclared peanut allergen resulting from a supplier's flour recall.
WalkMed Infusion is voluntarily recalling T100-000F IV sets due to the potential presence of particulate matter in or on the devices.
WalkMed Infusion is voluntarily recalling specific lots of 90-inch IV administration sets due to the potential presence of particulate matter in or on the devices.
Kellogg Company is voluntarily recalling Keebler Gripz Chips D 325 ct Bulk, .9 oz. because of the potential for undeclared peanut allergen.
WalkMed Infusion is voluntarily recalling specific lots of 90-inch IV administration sets due to the potential presence of particulate matter in or on the devices.
WalkMed Infusion is voluntarily recalling specific lots of IV sets with 0.22 micron filters due to the potential presence of particulate matter in or on the devices.
WalkMed Infusion is voluntarily recalling Triton Administration Sets due to the potential presence of particulate matter in or on the devices.
Biomet, Inc. is recalling 5,458 units of the TSP Hip Fracture Plating System because screws may fracture during implantation, potentially leaving a foreign body in the patient.
WalkMed Infusion is voluntarily recalling specific lots of Triton IV administration sets due to the potential presence of particulate matter in or on the devices.