State

North Carolina product recalls

72,984 recalls have nationwide distribution and so reach North Carolina. 10,261 additional recalls listed North Carolina specifically in their distribution scope.

What the numbers show

Total: 10,261
Critical: 1,476
Severe: 2,520
Most recent: 2026-09-09

Of the 10,261 recalls naming North Carolina we have scored against our rubric, 1,476 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,520 (25%) are Severe.

Which agencies issued them

These figures cover only the 10,261 recalls whose distribution notice names North Carolina specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6951–6975 of 83245

ModerateFDA (Drugs)·D-0433-2025·2025-05-28
Maximum Security Anticavity Toothpaste Sachets Recalled for CGMP Deviations
KENIL HEALTHCARE PRIVATE LIMITED is recalling Maximum Security Anticavity Gel Toothpaste sachets distributed in Delaware and North Carolina due to Current Good Manufacturing Practice (CGMP) deviations identified by the FDA.
Product
Maximum Security, Anticavity Gel Toothpaste, Sodium Fluoride 0.22%, Fresh Mint Flavor, NET WT 0.15 OZ (4.25 g) Sachets, Made in India, Dist. by Bob Barker Co. Inc., Fuquay-Varina, NC 27526, NDC 53247-132-01
Category
Drug
Distribution
2 states
ModerateFDA (Devices)·Z-1794-2025·2025-05-28
Philips Evolution Upgrade 3.0T MRI Cross Reference Line Alignment Error
Philips is recalling Evolution Upgrade 3.0T MRI systems (Models 782117 and 782143) due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Product
Product Name: Evolution Upgrade 3.0T; Model Numbers: (1) 782117, (2) 782143;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0438-2025·2025-05-28
Nature Mint Anticavity Fluoride Toothpaste Recall Due to Manufacturing Deviations
KENIL HEALTHCARE PRIVATE LIMITED is recalling Nature Mint Anticavity Fluoride Toothpaste (0.85 oz tubes) distributed in Delaware and North Carolina due to Current Good Manufacturing Practice (CGMP) deviations.
Product
Nature Mint Anticavity Fluoride Toothpaste, Sodium monofluorophosphate 0.76%, NET WT 0.85 OZ (24 grams) Tube, Made in India, Dist. by Bob Barker Co. Inc., Fuquay-Varina, NC 27526, NDC 53247-131-03
Category
Drug
Distribution
2 states
ModerateFDA (Devices)·Z-1797-2025·2025-05-28
Ingenia 3.0T MRI Systems Recalled for Image Alignment Errors
Philips is recalling certain Ingenia 3.0T MRI systems worldwide due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Product
Product Name: Ingenia 3.0T; Model Numbers: (1) 781342, (2) 781377, (3) 782103;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1793-2025·2025-05-28
Evolution Upgrade 1.5T imaging system alignment error recall
Philips Evolution Upgrade 1.5T medical imaging systems may display alignment errors in cross-reference line functionality when reviewing images via MobiView application.
Product
Product Name: Evolution Upgrade 1.5T; Model Numbers: (1) 782116, (2) 782148;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1795-2025·2025-05-28
Ingenia 1.5T MRI Systems Recalled for Alignment Errors
Philips is recalling Ingenia 1.5T MRI systems due to potential alignment errors in the cross reference line functionality when reviewing images with the MobiView application.
Product
Product Name: Ingenia 1.5T; Model Numbers: (1) 781315, (2) 781341, (3) 781396, (4) 782101, (5) 782115, (6) 782140;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0425-2025·2025-05-28
KOFAL Original Pain Relieving Ointment Recalled for CGMP Deviations
KENIL HEALTHCARE PRIVATE LIMITED is recalling KOFAL Original Penetrating Pain Relieving Ointment (methyl salicylate 12%) due to Current Good Manufacturing Practice (CGMP) deviations. The recall affects approximately 16,248 jars distributed in Delaware and North Carolina.
Product
KOFAL Original, Penetrating Pain Relieving Ointment (methyl salicylate 12% - Topical Analgesic), 4 oz (113 g) Jar, Distributed by: Pharmadel LLC, Georgetown, DE 199747, NDC 55758-106-04, UPC 8 9971100128 0.
Category
Drug
Distribution
2 states
ModerateFDA (Drugs)·D-0445-2025·2025-05-28
Indomethacin Extended-Release Capsules Recalled for cGMP Deviations
KVK Tech, Inc. is recalling Indomethacin Extended-Release Capsules USP, 75 mg (Lot #18400A) nationwide due to cGMP deviations. The recall affects approximately 9,107 bottles distributed nationwide.
Product
INDOMETHACIN — INDOMETHACIN (INDOMETHACIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0430-2025·2025-05-28
Cinnafresh Anticavity Gel Toothpaste Recalled Due to CGMP Deviations
Cinnafresh anticavity gel toothpaste (sodium fluoride 0.22%, Bold Cinnamon Flavor) is being recalled due to Current Good Manufacturing Practice (CGMP) deviations. The manufacturer, KENIL HEALTHCARE PRIVATE LIMITED, initiated this voluntary recall.
Product
Cinnafresh anticavity gel toothpaste, sodium fluoride 0.22%, Bold Cinnamon Flavor, NET WT. 0.85 OZ (24 grams) Tube, Made in India, Dist. by Bob Barker Co. Inc., Fuquay-Varina, NC 27526, NDC 53247-133-01
Category
Drug
Distribution
2 states
ModerateFDA (Drugs)·D-0422-2025·2025-05-28
Antifungal Drug Recalled for Manufacturing Process Deviations
Pharmadel LLC is recalling CURA HONGOS 1% Clotrimazole topical lotion due to Current Good Manufacturing Practice (CGMP) deviations identified during production. The voluntary recall affects approximately 10,128 bottles distributed in Delaware and North Carolina.
Product
CURA HONGOS, Antifungal, 1% Clotrimazole, Topical Lotion, 0.76 fl oz (22.5 mL) Bottle, Dist by/por: Pharmadel LLC, New Castle, DE 19720, Made in India, NDC 55758-34-01, UPC 8 10096 77170 4.
Category
Drug
Distribution
2 states
ModerateFDA (Drugs)·D-0429-2025·2025-05-28
Rapidol Triple Antibiotic Ointment Recalled for CGMP Deviations
Rapidol Triple Antibiotic First Aid Ointment (Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate) distributed in Delaware and North Carolina is being recalled for CGMP deviations. The manufacturer initiated a voluntary recall of 9,336 tubes.
Product
RAPIDOL — RAPIDOL (BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE)
Category
Drug
Distribution
2 states
ModerateFDA (Drugs)·D-0428-2025·2025-05-28
Rapidol Hydrocortisone 1% Anti-Itch Cream Recalled for CGMP Deviations
Kenil Healthcare is recalling 10,000 tubes of Rapidol Maximum Strength Hydrocortisone 1% Anti-Itch Cream (2 oz, Lot SP26A, Expiration 09/30/2026) distributed in Delaware and North Carolina due to manufacturing quality issues.
Product
RAPIDOL — RAPIDOL (HYDROCORTISONE)
Category
Drug
Distribution
2 states
ModerateFDA (Drugs)·D-0421-2025·2025-05-28
Artridon Topical Analgesic Recalled for Manufacturing Process Deviations
Kenil Healthcare is recalling 9,984 tubes of Artridon topical analgesic (menthol and methyl salicylate) due to Current Good Manufacturing Practice (CGMP) deviations. The recall affects units distributed in Delaware and North Carolina.
Product
ARTRIDON — ARTRIDON (MENTHOL, METHYL SALICYLATE)
Category
Drug
Distribution
2 states
ModerateFDA (Devices)·Z-1800-2025·2025-05-28
Ingenia 3.0T CX MRI System Alignment Error in Cross Reference Line
Philips is recalling the Ingenia 3.0T CX MRI system due to potential alignment errors in the cross reference line when using the MobiView application to review images. The alignment error could affect image accuracy during review.
Product
Product Name: Ingenia 3.0T CX; Model Number: 781271;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0424-2025·2025-05-28
Kingskin SacaCallos salicylic acid solution recalled for manufacturing deviations
Kingskin SacaCallos 17% salicylic acid bottles are being recalled due to manufacturing deviations. The firm initiated the voluntary recall affecting approximately 9,000 bottles distributed in Delaware and North Carolina.
Product
Kingskin, SacaCallos, 17% Salicylic acid, 0.5 fl oz (14.8mL) Bottle, Dist. by: Pharmadel LLC, New Castle, DE 19720, Made in India, NDC 55758-423-15, UPC 8 10096 77163 6.
Category
Drug
Distribution
2 states
ModerateFDA (Devices)·Z-1786-2025·2025-05-28
Check-Flo Performer Introducer medical device recall for incorrect sheath sizing
Cook Incorporated is recalling Check-Flo Performer Introducer devices (10.0Fr) because affected units may contain an incorrectly sized introducer sheath, which could compromise proper device function.
Product
Check=Flo Performer Introducer, 10.0Fr, Reference Part Number(RPN) REF RCFW-10.0-0-38-30-RB, Order Number (GPN) REF G08686,
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0435-2025·2025-05-28
Nature Mint Anticavity Fluoride Toothpaste Recalled for CGMP Deviations
KENIL HEALTHCARE PRIVATE LIMITED is recalling Nature Mint Anticavity Fluoride Toothpaste due to Current Good Manufacturing Practice (CGMP) deviations. The recall affects approximately 19,500 tubes distributed in Delaware and North Carolina.
Product
Nature Mint, Anticavity Fluoride Toothpaste, Sodium monofluorophosphate 0.76%, NET WT 4.6 OZ (130 grams) Tube, Made in India, Dist. by Bob Barker Co. Inc., Fuquay-Varina, NC 27526, NDC 53247-131-06
Category
Drug
Distribution
2 states
ModerateFDA (Drugs)·D-0439-2025·2025-05-28
Nature Mint Anticavity Fluoride Toothpaste Recalled for CGMP Deviations
KENIL HEALTHCARE PRIVATE LIMITED is recalling Nature Mint Anticavity Fluoride Toothpaste due to manufacturing deviations. The recall affects 150,768 tubes distributed in Delaware and North Carolina.
Product
Nature Mint Anticavity Fluoride Toothpaste, Sodium monofluorophosphate 0.76%, NET WT 1.5 OZ (43 grams) Tube, Made in India, Dist. by Bob Barker Co. Inc., Fuquay-Varina, NC 27526, NDC 53247-131-04
Category
Drug
Distribution
2 states
ModerateFDA (Drugs)·D-0434-2025·2025-05-28
Maximum Security Anticavity Gel Toothpaste recalled for CGMP deviations
Maximum Security Anticavity Gel Toothpaste (Sodium Fluoride 0.22%, Fresh Mint) distributed in Delaware and North Carolina is being recalled due to CGMP deviations identified by the manufacturer.
Product
Maximum Security, Anticavity Gel Toothpaste, Sodium Fluoride 0.22%, Fresh Mint Flavor, NET WT 1.5 OZ (43 g) Tube, Made in India, Dist. by Bob Barker Co. Inc., Fuquay-Varina, NC 27526, NDC 53247-132-04
Category
Drug
Distribution
2 states
ModerateFDA (Drugs)·D-0437-2025·2025-05-28
Nature Mint Anticavity Fluoride Toothpaste recall due to manufacturing deviations
KENIL HEALTHCARE PRIVATE LIMITED is recalling Nature Mint Anticavity Fluoride Toothpaste (6.4 oz, Lot B0067, expiring 08/31/2026) distributed in Delaware and North Carolina due to Current Good Manufacturing Practice (CGMP) deviations.
Product
Nature Mint, Anticavity Fluoride Toothpaste, Sodium monofluorophosphate 0.76%, NET WT 6.4 OZ (181 grams) Box, Made in India, Dist. by Bob Barker Co. Inc., Fuquay-Varina, NC 27526, NDC 53247-131-07
Category
Drug
Distribution
2 states
ModerateFDA (Devices)·Z-1806-2025·2025-05-28
Smith & Nephew Lag/Compression Screw Kit Undersized Socket Defect
Smith & Nephew is recalling a Lag/Compression Screw Kit (REF: 71642690) because some compression screws have undersized hexagon sockets that render them non-functional and require replacement.
Product
META-TAN LAG/COMPRESSION SCREW KIT 90MM/85MM, REF: 71642690
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1799-2025·2025-05-28
Philips Ingenia 1.5T CX MRI System Alignment Error Potential
Philips is recalling Ingenia 1.5T CX MRI systems due to potential alignment errors in the cross reference line functionality when reviewing images with the MobiView application. This could affect image interpretation.
Product
Product Name: Ingenia 1.5T CX; Model Number: 781262;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0423-2025·2025-05-28
Antifungal Cream Recalled for Manufacturing Deviations
Kenil Healthcare is recalling CURA HONGOS Antifungal Cream (Clotrimazole 1%, 2 oz tubes) distributed in Delaware and North Carolina due to CGMP (Current Good Manufacturing Practice) deviations detected during manufacturing.
Product
CURA HONGOS, Antifungal Cream, Clotrimazole 1%, Net Wt/ Peso Neto 2 oz (56.7g) Tube, Distributed by: Pharmadel LLC, New Castle, DE 19720, Made in India, UPC 8 997110 011052.
Category
Drug
Distribution
2 states
ModerateFDA (Drugs)·D-0443-2025·2025-05-28
Esomeprazole Magnesium oral suspension recalled for failed impurity specifications
Zydus Pharmaceuticals is recalling Esomeprazole Magnesium delayed-release oral suspension, 20 mg, due to out-of-specification test results for unknown degradation products detected during long-term stability testing.
Product
ESOMEPRAZOLE MAGNESIUM — ESOMEPRAZOLE MAGNESIUM (ESOMEPRAZOLE MAGNESIUM)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·25V351000·2025-05-27
Kia K5 parking lights can flicker due to a software error
Kia is recalling certain 2025 K5 vehicles because a software error in the Power-net Domain Controller may cause the parking lights to flicker, failing FMVSS 108.
Product
KIA — KIA K5
Category
Vehicle
Distribution
Distributed nationwide