State
73,738 recalls have nationwide distribution and so reach South Carolina. 7,152 additional recalls listed South Carolina specifically in their distribution scope.
Of the 7,152 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 2,169 (30%) are Severe.
Which agencies issued them
These figures cover only the 7,152 recalls whose distribution notice names South Carolina specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Zimmer Biomet is recalling 5,459,583 LPS-MOB Articular Surface Implants because non-highly polished implants may adhere to the LDPE bag.
Zimmer Biomet is recalling 5.4 million periarticular locking elbow plates because non-highly polished implants may adhere to the packaging bag.
Zimmer Biomet is recalling various surgical screws and reamers because non-highly polished implants may adhere to the LDPE bag.
Ortho-Clinical Diagnostics is recalling VITROS chemistry Cl- Slides because an anti-backup platen failure may cause intermittent slide dispense issues.
Zimmer Biomet is recalling femorotibial and femoral nails because non-highly polished implants may adhere to the previous LDPE packaging bag.
Zimmer Biomet is recalling 5,459,583 limb salvage arthroplasty devices because non-highly polished implants may adhere to the LDPE bag packaging.
Zimmer Biomet is recalling various fixation systems and accessories because non-highly polished implants may adhere to the LDPE bag.
Zimmer Biomet is recalling various knee systems because non-highly polished implants may adhere to the LDPE bag packaging.
LivaNova is recalling VNS Therapy System generators because a timing change causes reported lead impedance values to be higher than previous models, shifting normal ranges relative to existing thresholds.
Zimmer Biomet is recalling NCB-PH plates because non-highly polished implants may adhere to the LDPE bag packaging.
Zimmer Biomet is recalling Sidus Stem-Free Shoulder Humeral Head implants because non-highly polished units may adhere to the LDPE bag.
Zimmer Biomet is recalling Coorad Morrey Total Elbow implants because non-highly polished components may adhere to the packaging bag.
Owen Mumford USA is recalling 140 Petfine Auto Injectors due to a possible assembly error in the Autoject EI component.
Zimmer Biomet is recalling Metasul Taper Liners because non-highly polished implants may adhere to the LDPE bag. The recall covers devices manufactured prior to January 2014.
Zimmer Biomet is recalling Cable-Ready Short and Long GTR implants because non-highly polished units may adhere to the LDPE bag.
Zimmer Biomet is recalling Metasul Femoral Heads because non-highly polished implants may adhere to the LDPE bag packaging.
Biomedical Polymers is recalling Manual Diff Droppers because the metal cannula may break or fail to pierce blood specimen tubes.
Zimmer Biomet is recalling Trabecular Metal Reverse Shoulder System implants because non-highly polished components may adhere to the packaging bag.
Zimmer Biomet is recalling NCB Proximal Lateral Tibia implants because non-highly polished devices may adhere to the packaging bag.
Zimmer Biomet is recalling various knee systems because non-highly polished implants may adhere to the LDPE bag.
Zimmer Biomet is recalling BF Humeral Stems because non-highly polished implants may adhere to the LDPE bag packaging.
Zimmer Biomet is recalling 5.4 million cephalomedullary nails because non-highly polished implants may adhere to the packaging bags.
Zimmer Biomet is recalling Prox Lat Humeral Lock Plates because non-highly polished implants may adhere to the LDPE bag packaging.
Zimmer Biomet is recalling 5,459,583 Connection Screws for NCB Plates because non-highly polished implants may adhere to the LDPE bag.
Zimmer Biomet is recalling 5.4 million ankle implants because non-highly polished devices may adhere to the packaging bag.