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.

1451–1475 of 80023

SevereFDA (Devices)·Z-2253-2026·2026-06-10
BD combined Whitacre and Quincke spinal trays recalled over bupivacaine
BD Spinal Trays containing both a Whitacre 25 G and a Quincke 22 G needle are being recalled as a sub-recall of the Huons bupivacaine product recall. 290 units affected.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in., BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405741.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2250-2026·2026-06-10
BD Quincke 26G spinal trays recalled in Huons bupivacaine sub-recall
BD Spinal Trays with Quincke needle 26 G, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall. 890 units are affected.
Product
BD¿Spinal Tray with BD¿Quincke Needle 26 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405632.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2223-2026·2026-06-10
Ivenix pump software may report false battery health and shut down
The Ivenix Infusion System Large Volume Pump software is being recalled because a software anomaly can report a false battery-health value and trigger a shutdown alarm.
Product
LVP software of the Ivenix Infusion System (IIS); Product Code LVP-SW-0005.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2257-2026·2026-06-10
BD Whitacre 25G spinal trays recalled in Huons bupivacaine sub-recall
BD Spinal Trays with Whitacre needle 25 G, catalog numbers 405637 and 405707, are being recalled as a sub-recall of the Huons bupivacaine product recall. 5,940 units are affected.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 405637, 405707.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0910-2026·2026-06-10
Cold prep cream sauce contains dry milk recalled for Salmonella
Cold Prep Cream Sauce in 20 lb bags is being recalled because it contains a dry milk powder ingredient recalled by the supplier over potential Salmonella contamination.
Product
Cold Prep Cream Sauce, 20 lb., packaged in a tied poly bag and packed 1 bag per case, UPC 0039954922458
Category
Food
Distribution
41 states
SevereFDA (Devices)·Z-2277-2026·2026-06-10
Spinocan spinal needle kits recalled over Huons bupivacaine quality issues
Spinocan spinal needle procedure kits are being recalled because they contain Bupivacaine Hydrochloride in Dextrose Injection subject to the Huons recall. 16,080 units affected.
Product
Spinocan Spinal Needle procedure kits: Material Description (Material Number): Spinocan 26 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333201); Spinocan 25 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333211); Spin
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2224-2026·2026-06-10
Ivenix infusion pumps may hide internal damage after being dropped
Ivenix Infusion System Large Volume Pumps are being recalled because dropping or jarring can loosen the touchscreen input cable, causing random touches or an unresponsive screen.
Product
Ivenix Infusion System (IIS), Large Volume Pump, Model Number: LVP-0004
Category
Medical Device
Distribution
21 states
SevereFDA (Devices)·Z-2248-2026·2026-06-10
BD Quincke spinal trays recalled over Huons bupivacaine quality issues
BD Spinal Trays with a Quincke 22 G needle are being recalled as a sub-recall of the Huons bupivacaine product recall. 990 units are affected.
Product
BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405609.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2249-2026·2026-06-10
BD Quincke 25G spinal trays recalled in Huons bupivacaine sub-recall
BD Spinal Trays with Quincke needle 25 G, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall. 3,130 units are affected.
Product
BD¿Spinal Tray with BD¿Quincke Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 405621, 405735.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2255-2026·2026-06-10
BD Whitacre spinal trays across nine catalog numbers recalled over bupivacaine
BD Spinal Trays with Whitacre needle 25 G, spanning nine catalog numbers, are being recalled as a sub-recall of the Huons bupivacaine product recall. 13,320 units affected.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 400866, 405672, 405673, 405674, 405675, 405709, 405721, 405723, 406704.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2278-2026·2026-06-10
Design Options spinal trays recalled over Huons bupivacaine quality issues
Design Options spinal needle anesthesia procedure kits are being recalled because they contain Bupivacaine Hydrochloride in Dextrose Injection subject to the Huons recall.
Product
Design Options Spinal Tray Spinal Needle Anesthesia procedure kits: Material Description (Material Number): SSK H M C 20061890 (560074), SSK S C H (560214), SSK BJC H S (ORIGINAL CUST) (560272), SSK CA P M C (ORIGINAL CUST) (560327), SSK T M H (560394), SSK S O 20070208 (
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2276-2026·2026-06-10
B. Braun spinal needle kits recalled over Huons bupivacaine quality issues
Spinal needle procedure kits containing Bupivacaine Hydrochloride in Dextrose Injection are being recalled after the drug's manufacturer issued a voluntary recall. 582,030 units are affected.
Product
Spinal Needle procedure kits: Material Description (Material Number) 24GA. PENCAN SPINAL BUP. TRAY W/DURAPREP (333867); 25GA. PENCAN SPINAL BUP. TRAY W/DURAPREP (333862); GOVP24BK 24G PENCAN TRAY W/ BUP & DEXTROS (332607); P24BK 24G PENCAN TRAY W/BUP & DEXTROSE (333868); P
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0908-2026·2026-06-10
Aramark cheese sauce contains dry milk powder recalled over Salmonella
Aramark Cheese Sauce New & Improved in 25 lb bags is being recalled because it contains a dry milk powder ingredient recalled by the supplier over potential Salmonella contamination.
Product
Aramark Cheese Sauce New & Improved, 25 lb., packaged in a tied poly bag and packed 2 bags per case, UPC 0039954925121
Category
Food
Distribution
41 states
SevereFDA (Devices)·Z-2254-2026·2026-06-10
BD Whitacre 25 gauge spinal trays recalled over bupivacaine quality issues
BD Spinal Trays with a Whitacre 25 G needle, catalog number 405658, are being recalled as a sub-recall of the Huons bupivacaine product recall. 150 units affected.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 2 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405658.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2291-2026·2026-06-10
Philips Azurion 7M20 Roadmap Pro may produce unusable dark images
Philips Azurion 7M20 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.
Product
Philips Azurion 7M20, Model Numbers: 722079, 722224 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1038-2026·2026-06-10
Albertsons kale berry feta salad does not declare walnut
Albertsons store-made Kale Berry Feta Salad is being recalled because the contains statement does not declare walnut. 31 units are affected.
Product
UPC 29472300000 SALAD KALE BERRY FETA FS COLD UPC 29472100000 Ready Meals SALAD KALE BERRY FETA SS COLD This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-1031-2026·2026-06-10
Albertsons lox avocado toast does not declare salmon allergen
Albertsons store-made Lox Avocado Toast is being recalled because the contains statement does not declare salmon. 19 units are affected.
Product
UPC 21299900000 LOX AVOCADO TOAST FS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2288-2026·2026-06-10
Philips Azurion 7B12 Roadmap Pro may produce unusable dark images
Philips Azurion 7B12/12 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.
Product
Philips Azurion 7B12/12, Model Numbers: 722067, 722225 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2303-2026·2026-06-10
BD Pyxis MedBank Tower fingerprint scanner may overheat and burn
The BD Pyxis MedBank Tower medication cabinet is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.
Product
BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2304-2026·2026-06-10
BD Pyxis MedBank Mini fingerprint scanner may overheat and burn
The BD Pyxis MedBank Mini medication cabinet is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.
Product
BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0565-2026·2026-06-10
CareOne extra strength calcium antacid tablets contain metallic particles
CareOne Extra Strength Calcium Antacid, calcium carbonate 750 mg, is being recalled because of the presence of small metallic particles in the chewable tablets.
Product
EXTRA STRENGTH ANTACID — EXTRA STRENGTH ANTACID (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0955-2026·2026-06-10
Albertsons cravin carrot cake does not declare pecan allergen
Albertsons store-made Cake Cravin Carrot 8-inch 1-layer is being recalled because the contains statement does not declare pecan. 138 units are affected.
Product
UPC 22679400000 CAKE CRAVIN CARROT 8IN 1-layer This is Albertson's store-made item and is sold by each unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-1020-2026·2026-06-10
Albertsons chicken strip salad does not declare almond allergen
Albertsons store-made Kitchen Salad Chicken Strip is being recalled because the contains statement does not declare almond. 55 units are affected.
Product
UPC 29433900000 Kitchen SALAD CHICKEN STRIP This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2299-2026·2026-06-10
BD Pyxis Anesthesia Station fingerprint scanner may overheat and burn
The BD Pyxis Anesthesia Station ES is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn. 4,579 units affected.
Product
BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1000-2026·2026-06-10
Albertsons shrimp and surimi ceviche does not declare sea bream
Albertsons store-made Shrimp & Surimi Ceviche Fresh is being recalled because the contains statement does not declare sea bream. 315 units are affected.
Product
UPC 23245700000 SHRIMP & SURIMI CEVICHE FRESH This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide