State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Smith & Nephew is recalling Renovation Thin Osteotome Blades because stability data does not support the labeled 10-year shelf life.
The Anspach Effort, Inc. is recalling 554 XMAX Pneumatic Drill Systems because the supplied directions for use did not include a recommended service interval.
Smith & Nephew is recalling Renovation osteotome blades because stability data does not support the labeled 10-year shelf life.
The Anspach Effort, Inc. is recalling eight Green Rotating Craniotomes because the supplied directions for use did not contain a recommended service interval.
The Harvard Drug Group is recalling 2,341 cartons of Fluconazole 100 mg tablets because they failed to meet dissolution specifications.
Threshold Enterprises Ltd is recalling specific lots of Source Naturals Vitamin D-3 dietary supplements because testing found lower concentrations than labeled.
The Anspach Effort, Inc. is recalling 22 SC2100 foot controls because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 58 Bearing Sleeve units because the supplied directions for use did not contain a recommended service interval.
Smith & Nephew is recalling specific lots of Renovation Radial Osteotome Blades because stability data does not support the labeled 10-year shelf life.
Akorn Inc is recalling 55,968 bottles of Sulfamethoxazole and Trimethoprim Oral Suspension because the product failed to meet dissolution specifications.
The Anspach Effort, Inc. is recalling 224 Bearing Sleeves because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 239 System Console units because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 10.5cm Long Attachments for pneumatic systems because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 41 units of the 19cm Attachment, Black Max, because the supplied directions for use did not include a recommended service interval.
The Anspach Effort, Inc. is recalling 198 units of the 7.2cm Adjustable Drill Guide because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 22 Minimal Access Attachments because the supplied directions for use did not contain a recommended service interval.
Breg Inc is recalling approximately 2,609 sterile dressings because a small percentage may have unsealed pouches, rendering them non-sterile.
The Anspach Effort, Inc. is recalling 206 units of the 20.2cm Heavy Duty Long Heavy Short Attachment because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling six units of the Adjustable Drill Guide, Black Max because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 148 Standard Craniotomes because the supplied directions for use did not include a recommended service interval.
The Anspach Effort, Inc. is recalling 17 units of the 16.5cm Micro Revision Attach because the supplied directions for use did not include a recommended service interval.
The Anspach Effort, Inc. is recalling 14 IMRI Short Attachment units because the supplied directions for use did not include a recommended service interval.
Breg Inc is recalling 2,609 units of If Hip Sterile Polar Dressings because some may have unsealed pouches, rendering them non-sterile.
The Anspach Effort, Inc. is recalling three Pediatric Craniotomes because the supplied directions for use did not contain a recommended service interval.
The Anspach Effort, Inc. is recalling 98 Minimal Access Straight Drivers because the supplied directions for use did not contain a recommended service interval.