State

South Carolina product recalls

73,597 recalls have nationwide distribution and so reach South Carolina. 7,146 additional recalls listed South Carolina specifically in their distribution scope.

What the numbers show

Total: 7,146
Critical: 1,275
Severe: 2,169
Most recent: 2026-10-14

Of the 7,146 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 7,146 recalls whose distribution notice names South Carolina specifically. The 73,597 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1951–1975 of 80743

HighFDA (Devices)·Z-2476-2026·2026-06-24
Giraffe OmniBed Carestation canopy fasteners can fall into patient compartment
Giraffe OmniBed Carestations are being recalled because fasteners securing the canopy soffit can disengage and fall into the patient compartment. 23,430 units affected.
Product
Giraffe OmniBed Carestations and Giraffe OmniBed Carestation CS1, a combination of an infant incubator and an infant warmer, Model Numbers 2082844-001-XXX
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2504-2026·2026-06-24
Medline D and C and cardiovascular packs contain substandard catheters
Medline D and C Packs and a custom cardiovascular pack are being recalled because representative samples did not meet applicable catheter performance specifications. 168 units affected.
Product
MEDLINE Medical Procedure Kits labeled as: 1) D AND C PACK, Medline Kit Number/SKU DYNJ53973C; 2) PK CUST CV A&B CABRINI CO, Medline Kit Number/SKU DYNJ60583C.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2505-2026·2026-06-24
Medline gynaecology procedure packs contain catheters failing performance specifications
Medline gynaecology procedure packs including hysteroscopy, D&C and tubal ligation kits are being recalled because sample catheters did not meet performance specifications. 37,324 units affected.
Product
MEDLINE Medical Procedure Kits labeled as CLOVIS HYSTEROSCOPY, CSC-N PELVISCOPY, D AND C PACK, D&C HYSTER PACK, FLWR GYN PACK, FS LAP TUBAL LIGATION, HILLSDALE D&C / HYSTEROSCOPY, LAVH NEW BRAUNFELS,TVH PACK, etc (see recall documents for a full list of affected products)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2494-2026·2026-06-24
Medline tonsil packs contain catheters failing performance specifications
Medline Tonsil Pack Cath procedure kits are being recalled because representative samples did not meet applicable catheter performance specifications. 384 units are affected.
Product
MEDLINE Medical Procedure Kits labeled as: TONSIL PACK CATH, Medline Kit Number/SKU DYNJ65199A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2464-2026·2026-06-24
ConMed AirSeal 5mm smooth access ports may trigger overpressure alerts
ConMed AirSeal 5 mm Smooth Access Ports and Obturators with Blunt Tip are being recalled because of the potential for overpressure alerts. 497 packs, or 2,982 units, are affected.
Product
ConMed AirSeal 5 mm Smooth Access Port and Obturator with Blunt Tip, 150mm Length. Catalog Number: iASB5-150. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2486-2026·2026-06-24
Medline cardiac surgery and ECMO packs contain substandard catheters
Medline cardiac procedure kits including basic heart, cardiac surgery, carotid endarterectomy and ECMO packs are being recalled over catheter specification failures. 4,801 units affected.
Product
MEDLINE Medical Procedure Kits labeled as: 1) BASIC HEART PACK, Medline Kit/SKU DYNJ67331B; 2) CARDIAC SURGERY, Medline Kit/SKU DYNJ911589A; 3) CAROTID ENDARTECOMY, Medline Kit/SKU DYNJ36211D; 4) CHLA ECMO / CARDIAC PACK, Medline Kit/SKU DYNJ87973; 5) CHLA ECMO…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2497-2026·2026-06-24
Medline bioburden test and cystectomy kits contain substandard catheters
Medline procedure kits including the Bioburden Test Kit and Kit Uro Robot Cystectomy are being recalled because sample catheters did not meet performance specifications. 123,030 units affected.
Product
MEDLINE Medical Procedure Kits labeled as BIOBURDEN TEST KIT, Kit Uro Robot Cystectomy, etc. (see the recall documents for a full list of products)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0594-2026·2026-06-24
Aripiprazole 30mg bottle contained voriconazole 50mg tablets instead
Aripiprazole Tablets USP 30 mg from Ajanta Pharma are being recalled after a bottle containing Voriconazole Tablets 50 mg was labelled and distributed as aripiprazole. 6,143 bottles affected.
Product
ARIPIPRAZOLE — ARIPIPRAZOLE (ARIPIPRAZOLE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2475-2026·2026-06-24
Giraffe OmniBed incubator canopy fasteners can fall into patient compartment
Giraffe OmniBed incubator-warmers, all models, are being recalled because fasteners securing the canopy soffit can disengage and fall into the patient compartment. 19,587 units affected.
Product
Giraffe OmniBed, a combination of an infant incubator and an infant warmer, All Models
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2503-2026·2026-06-24
Medline gynaecology laparoscopy packs contain catheters failing performance specifications
Medline gynaecology procedure kits including basic GYN, D&C hysteroscopy and GYN laparoscopy packs are being recalled over catheter specification failures. 44,656 units affected.
Product
MEDLINE Medical Procedure Kits labeled as BASIC GYN, CW LAP GYN, D&C HYSTEROSCOPY, CW LAP GYN, DEACONESS PELVIC LAP PACK, FLOYD LAP GYN, GYN LAP PACK, GYN LAPAROSCOPY, GYN MINOR PACK, etc. (see the recall documents for a full list of affected products)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2495-2026·2026-06-24
Medline urethroplasty kits contain catheters failing performance specifications
Medline urology urethroplasty procedure kits are being recalled because representative samples did not meet applicable catheter performance specifications. 91 units are affected.
Product
MEDLINE Medical Procedure Kits labeled as: 1) KIT UROLOGY URETHROPLASTY, Medline Kit Number/SKU DYKMBNDL117C; 2) URETHROPLASTY, Medline Kit Number/SKU DYNJ908978; 3) URETHROPLASTY, Medline Kit Number/SKU DYNJ908978F.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0949-2026·2026-06-24
Great Value Hawaiian Rolls Recalled Due to Oily Packaging Substance
United States Bakery is recalling Great Value Hawaiian Rolls due to an oily and sticky substance found on the packaging's food contact surface. The product was never sold to consumers and all affected product has been accounted for.
Product
Great Value Hawaiian Roll 4pk, Item # F63384. Product is perishable dinner roll ready to eat, sold in a corrugated case of 18 packages (4.5oz net wt.) individually wrapped in laminated film. This product was never sold in stores and was never available for consumer purchase.…
Category
Food
Distribution
26 states
HighNHTSA·26V401000·2026-06-24
Airstream Recalls 2025-2027 Vehicles Due to Rooftop Fan Fire Risk
Airstream is recalling 2025-2027 Interstate and 2026 Classic recreational vehicles because a rooftop ventilation fan component may overheat and cause a fire.
Product
AIRSTREAM — AIRSTREAM INTERSTATE, CLASSIC
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2466-2026·2026-06-24
ConMed AirSeal 12mm blunt tip 100mm ports may trigger overpressure alerts
ConMed AirSeal 12 mm Access Ports and Obturators with Blunt Tip, 100 mm length, are being recalled because of the potential for overpressure alerts. 1,261 packs affected.
Product
ConMed AirSeal 12mm Access Port and Obturator with Blunt Tip, 100mm Length. Catalog Number: iASB12-100. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2487-2026·2026-06-24
Medline open heart and cardiac kits contain catheters failing specifications
Medline open heart and cardiac procedure kits are being recalled because representative samples did not meet applicable catheter performance specifications. 168,968 units are affected.
Product
MEDLINE Medical Procedure Kits labeled as CH OPEN HEART, ADULT CARDIAC KIT, AHT CVOR CABG, APH EMERGENCY OPEN HEART PACK, Etc. (see recall documents for a full list of products)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2468-2026·2026-06-24
ConMed AirSeal 8mm 100mm optical obturator ports may trigger overpressure alerts
ConMed AirSeal 8 mm Access Ports with Low Profile Bladeless Optical Tip Obturators, 100 mm length, are being recalled because of the potential for overpressure alerts.
Product
ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS8-100LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2489-2026·2026-06-24
Medline vasectomy reversal kits contain catheters failing performance specifications
Medline Bilateral Micro Vasectomy Reversal kits are being recalled because representative samples did not meet applicable catheter performance specifications. 588 units affected.
Product
MEDLINE Medical Procedure Kits labeled as: BILAT MICRO VASECTOMY REVERSAL, Medline Kit Number/SKU DYNJ68302
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2462-2026·2026-06-24
Stryker Triathlon size 4 baseplate packaging contained a size 3 implant
Triathlon Universal Baseplate Size 4 packaging is being recalled after Stryker identified that it contained a Size 3 baseplate, and vice versa. Seven units are affected.
Product
TRI TS BASEPLATE SIZE 4. Part Number: 5521-B-400.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2470-2026·2026-06-24
ConMed AirSeal 5mm 120mm optical obturator ports may trigger overpressure alerts
ConMed AirSeal 5 mm Access Ports with Low Profile Bladeless Optical Tip Obturators, 120 mm length, are being recalled because of the potential for overpressure alerts.
Product
ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120mm Length. Catalog Number: iAS5-120LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2471-2026·2026-06-24
ConMed AirSeal 5mm 100mm optical obturator ports may trigger overpressure alerts
ConMed AirSeal 5 mm Access Ports with Low Profile Bladeless Optical Tip Obturators, 100 mm length, are being recalled because of the potential for overpressure alerts.
Product
ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS5-100LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2469-2026·2026-06-24
ConMed AirSeal 5mm 75mm optical obturator ports may trigger overpressure alerts
ConMed AirSeal 5 mm Access Ports with Low Profile Bladeless Optical Tip Obturators, 75 mm length, are being recalled because of the potential for overpressure alerts.
Product
ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 75mm Length. Catalog Number: iAS5-75LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0596-2026·2026-06-24
Buprenorphine injection vials show crystallization identified as buprenorphine free base
Buprenorphine HCl Injection, 0.3 mg/mL single dose vials, is being recalled because of crystallization identified as buprenorphine free base. 46,334 units are affected.
Product
BUPRENORPHINE HYDROCHLORIDE — BUPRENORPHINE HYDROCHLORIDE (BUPRENORPHINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2499-2026·2026-06-24
Medline nursing kits contain catheters failing applicable performance specifications
Medline Nursing Kits, SKU EDUC1044, are being recalled because representative samples did not meet applicable catheter performance specifications. 730 units are affected.
Product
MEDLINE Medical Procedure Kits labeled as: NURSING KIT, Medline Kit Number/SKU EDUC1044
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2491-2026·2026-06-24
Medline tracheostomy and tonsil kits contain catheters failing specifications
Medline procedure kits including adult tracheostomy tube insertion, T&A and ear packs are being recalled because sample catheters did not meet performance specifications. 217,390 units affected.
Product
MEDLINE Medical Procedure Kits labeled as: ADULT TRACHEOSTOMY TUBE INSERT, ASC T&A, CONWAY T&A SINUS, EAR PACK, etc. (see the recall documents for the full list of products)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0634-2026·2026-06-24
Cura Hongos clotrimazole cream recalled over manufacturing practice deviations
Cura Hongos Crema Antifungica, clotrimazole 1%, in 2 oz tubes is being recalled because of CGMP deviations and deficiencies observed during an FDA inspection. 84 tubes affected.
Product
Cura Hongos, Crema Antifungica, Clotrimazole 1%, 2oz (57g) tubes, Dist by/por: Pharmadel LLC, New Castle, DE 19720, Made in India, UPC 8 52924 00683 1.
Category
Drug
Distribution
Distributed nationwide