State

South Carolina product recalls

72,907 recalls have nationwide distribution and so reach South Carolina. 7,116 additional recalls listed South Carolina specifically in their distribution scope.

What the numbers show

Total: 7,116
Critical: 1,268
Severe: 1,870
Most recent: 2026-09-09

Of the 7,116 recalls naming South Carolina we have scored against our rubric, 1,268 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,870 (26%) are Severe.

Which agencies issued them

These figures cover only the 7,116 recalls whose distribution notice names South Carolina specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

901–925 of 80023

SevereFDA (Devices)·Z-2463-2026·2026-07-08
Ventilator breathing circuit sets may obstruct exhalation valve
Hamilton Medical AG is recalling coaxial breathing circuit sets used with three ventilator models because membranes may stick to the expiratory valve body, preventing proper gas exhalation and potentially causing inadequate ventilation.
Product
Breathing circuit set, coaxial: REF: 260127, 260128, 260167, 260168 used with HAMILTON-C1, HAMILTON-T1 and HAMILTON-MR1 ventilators.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2634-2026·2026-07-08
Boston Scientific CRE Wireguided Medical Device Recall Sterile Breach
Boston Scientific is recalling CRE Wireguided 10-12mm 240cm medical devices due to a potential sterile breach in the product packaging. The breach could compromise device sterility and affect patient safety.
Product
CRE Wireguided 10-12mm 240cm
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2551-2026·2026-07-08
Hillrom VOLARA System patient circuits recalled for nebulizer cup leakage
Baxter Healthcare is recalling Hillrom VOLARA System patient circuits due to reports of air and medication leakage from the nebulizer cup, which can cause oxygen level drops and ineffective medication delivery.
Product
Hillrom VOLARA System P.CIRCUIT 5KIT AC, (Single Patient Use Circuit), Model/Catalog Number REF M08474; Oscillation Lung Expansion Therapy, positive pressure breathing device
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0645-2026·2026-07-08
ChloraPrep One-Step Applicators Recalled Due to Sterility Assurance Failure
CareFusion 213, LLC is recalling ChloraPrep One-Step applicators nationwide because unsterilized units intended for further processing were distributed to customers outside the intended distribution channel, lacking sterility assurance.
Product
CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2603-2026·2026-07-08
Omnipod 5 Insulin Infusion Pods Recalled for External Cannula Damage
Insulet Corporation is recalling approximately 4.9 million Omnipod 5 insulin pods due to external soft cannula damage during manufacturing that can cause insulin leakage and under-delivery, potentially leading to high blood glucose and serious diabetic complications.
Product
Omnipod 5 Pods. Includes the below Model/REF Numbers: 1. POD-OMNI-I1-6720. 2. POD-OMNI-I1-6220. 3. OMNI-I1-6729 (10-Pack), OMNI-I1-6720 (Single Pod). 4. OMNI-I1-6220. 5. OMNI-I1-6720. 6. BLE-H1-529 (10-Pack), BLE-H1-520 (Single Pod).
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2620-2026·2026-07-08
Thyroid FNA Pack-RX Surgical Kit Recalled for Bacterial Contamination
Windstone Medical Packaging is recalling AMS Thyroid FNA Pack-RX surgical kits due to contamination with Paenibacillus phoenicis bacteria found in included Webcol alcohol prep pads.
Product
A M S, ALIGNED MEDICAL SOLUTIONS, Thyroid FNA Pack-RX, Pack Number AMS17729, surgical convenience kit
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2606-2026·2026-07-08
Medline Convenience Kits with Swan-Ganz Catheters Recalled
Medline Industries is recalling convenience kits containing Swan-Ganz catheters due to leaks and breakage of the proximal injectate lumen hub, which may cause infection, medication loss, or blood loss.
Product
Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT HEART CATH PACK CTX DYNJ68530B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2611-2026·2026-07-08
Medline Convenience Kits with Recalled Swan-Ganz Catheters Nationwide
Medline is recalling convenience kits containing Swan-Ganz catheters with a defective proximal injectate lumen hub that may leak, break, or cause infection and blood loss.
Product
Medline Convenience kits containing recalled Swan-Ganz Catheters OPEN HEART DYNJ909090B OPEN HEART CDS QVH CDS982523M
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2629-2026·2026-07-08
Boston Scientific CRE Pro Wireguided 12-15mm Esophageal Stent Recall
Boston Scientific is recalling CRE Pro Wireguided 12-15mm 240cm esophageal stents due to a potential sterile breach in the device packaging. Affected units were distributed worldwide.
Product
CRE Pro Wireguided 12-15mm 240cm
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2618-2026·2026-07-08
Medacta Short Monobloc Stem Broaches Surgical Instruments Shoulder Implant
Medacta USA is recalling Short Monobloc Stem Broaches used in shoulder replacement surgery due to positioning misalignment that may increase risk of fracture in the upper arm bone.
Product
Short Monobloc Stem Broaches, Size/REF: 7/04.01.10.0970, 8/04.01.10.0971, 9/04.01.10.0972, 10/04.01.10.0973, 11/04.01.10.0974, 12/04.01.10.0975, 13/04.01.10.0976, 14/04.01.10.0977, 15/04.01.10.0978, 16/04.01.10.0979 Part of Medacta Shoulder System
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V442000·2026-07-08
PETERBILT 579 Tractors Recalled for Air Brake Valve Installation
PACCAR is recalling certain 2026–2027 Peterbilt 579 and 2027 Kenworth T680 tractors with a potentially incorrectly installed trailer air connection quick release valve that can cause trailer instability after braking.
Product
PETERBILT — PETERBILT, KENWORTH 579, T680
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2628-2026·2026-07-08
CRE Pro Wireguided medical device sterile packaging breach recall
Boston Scientific Corporation is recalling the CRE Pro Wireguided 10-12mm 240cm device due to potential sterile breach of the pouches in which devices are packaged. The affected product has been distributed worldwide.
Product
CRE Pro Wireguided 10-12mm 240cm
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2639-2026·2026-07-08
Pilling Wecksorb Neurosponges Surgical Sponges Recalled for Endotoxin Contamination
Teleflex LLC is recalling Pilling Wecksorb Neurosponges and Neurosponge Strips due to out-of-specification or potentially out-of-specification endotoxin levels. The cotton surgical sponges are used in brain and spine surgery.
Product
Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling¿ Wecksorb Neurosponge Strips (Cotton) Model/Catalog Number: 200100 200101 200102 200103 200104 200105 200106 200108 200110 200112 200120 200121 200123 200131 Software V
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2643-2026·2026-07-08
ARTIS icono floor Medical Imaging System Detector Movement Loss Recall
Siemens Medical Solutions is recalling 30 units of the ARTIS icono floor (Model 11327700) due to potential loss of detector movement capability when adjusted to maximum or minimum height limits.
Product
ARTIS icono floor. Model Number: 11327700.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0660-2026·2026-07-08
Amphetamine extended-release capsules contain immediate-release pellets after label mix-up
Mixed amphetamine salts extended-release capsules, 5 mg, from Lannett are being recalled because the capsules contain only immediate-release pellets. 1,392 bottles affected.
Product
DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE — DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE (DEXTROAMPHETAMINE SULFATE, DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE SULFATE AND AMPHETAMINE ASPARTATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0655-2026·2026-07-08
Prednisolone Acetate Ophthalmic Suspension Recalled for Foreign Substance
Lupin Pharmaceuticals is recalling Prednisolone Acetate Ophthalmic Suspension, USP, 1% due to the presence of a foreign substance. Affected lot numbers were distributed nationwide.
Product
PREDNISOLONE ACETATE — PREDNISOLONE ACETATE (PREDNISOLONE ACETATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2625-2026·2026-07-08
IntelliCuff Portable Automatic Cuff Pressure Controller Recall
Hamilton Medical AG is recalling the IntelliCuff portable automatic cuff pressure controller due to a reported "Cuff System Leakage" error that may cause the motor to pump continuously and fail to maintain user-set cuff pressure.
Product
IntelliCuff, Portable automatic cuff pressure controller REF: 951001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2670-2026·2026-07-08
Radius VSM ECG Pre-connected Set Recalled for Incorrect Heart Rate Detection
Masimo Corporation is recalling Radius VSM ECG pre-connected sets because the ECG electrode assembly may incorrectly detect extreme bradycardia or tachycardia and trigger false alarms on patients with normal heart rates, potentially distracting clinicians from true positive alarms and delaying treatment.
Product
Radius VSM ECG pre-connected Set, REF: 4842, 4695
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V440000·2026-07-08
Shyft Recalls Utilimaster Velocity Vehicles Due to Strobe Light Fire Risk
Shyft Group is recalling 2016, 2019, and 2021 Utilimaster Velocity vehicles because water entering an improperly sealed strobe light may cause a short circuit and increase the risk of fire.
Product
UTILIMASTER — UTILIMASTER VELOCITY
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2623-2026·2026-07-08
GC Agar Base Culture Media Reduced Recovery of Neisseria gonorrhoeae
Remel, Inc is recalling GC Agar Base culture media because some strains of Neisseria gonorrhoeae may not be recovered or may show reduced recovery on the product.
Product
GC Agar Base (150mm) 10/PK R04030; GC Agar Base (100mm) 10/PK R01460
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1129-2026·2026-07-08
MorningStar Farms Buffalo Chik'n Nuggets recalled for potential plastic contamination
MorningStar Farms Buffalo Chik'n Nuggets (10.5 oz.) are being recalled due to potential contamination with plastic material. Affected products have Best If Used By dates of JUL 07 2027 and JUL 08 2027.
Product
MorningStar Farms Buffalo Chik'n Nuggets, 100% Plant Protein Vegan Nuggets, Net Wt. 10.5 oz. (298g), packaged in a resealable plastic bag with UPC 028989101105, packed 6 bags per case
Category
Food
Distribution
41 states
HighFDA (Food)·H-1130-2026·2026-07-08
MorningStar Farms Hot & Spicy Sausage Patties Recalled for Plastic Contamination
Mars Snacking is recalling MorningStar Farms Hot & Spicy Sausage Patties due to potential contamination with plastic material. The recall affects 17,218 cases distributed across 40 U.S. states and Puerto Rico.
Product
MorningStar Farms Hot & Spicy Sausage Patties, 100% Plant Protein Vegan Sausage Patties, Net Wt. 8 oz. (228g), packaged in a resealable plastic bag with UPC 028989100948, packed 6 bags per case
Category
Food
Distribution
41 states
HighFDA (Devices)·Z-2637-2026·2026-07-08
CRE Wireguided 18-20mm 240cm medical devices recalled for sterile breach
Boston Scientific Corporation is recalling CRE Wireguided 18-20mm 240cm devices worldwide due to a potential sterile breach of the pouches in which the devices are packaged.
Product
CRE Wireguided 18-20mm 240cm
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2612-2026·2026-07-08
Medline Convenience Kits with Recalled Swan-Ganz Catheters
Medline Convenience kits containing recalled Swan-Ganz catheters may leak or break at the proximal injectate lumen hub, risking infection, medication loss, and blood loss.
Product
Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT HEART CATH PACK CTX DYNJ68530A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2609-2026·2026-07-08
Medline Convenience Kits Containing Recalled Swan-Ganz Catheters
Medline is recalling convenience kits containing Swan-Ganz catheters due to leaks and breakage of the proximal injectate lumen hub, which may cause infection, medication loss, or blood loss.
Product
Medline Convenience kits containing recalled Swan-Ganz Catheters KIT GERMANTOWN CABG DYNJ905855 KIT UNIVERSITY CABG PACK DYNJ905857 OH MED RN CDS DYNJ905936B
Category
Medical Device
Distribution
Distributed nationwide