State

North Carolina product recalls

73,092 recalls have nationwide distribution and so reach North Carolina. 10,294 additional recalls listed North Carolina specifically in their distribution scope.

What the numbers show

Total: 10,294
Critical: 1,486
Severe: 2,536
Most recent: 2026-09-23

Of the 10,294 recalls naming North Carolina we have scored against our rubric, 1,486 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,536 (25%) are Severe.

Which agencies issued them

These figures cover only the 10,294 recalls whose distribution notice names North Carolina specifically. The 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9401–9425 of 83386

CriticalFDA (Devices)·Z-0382-2025·2024-11-27
Baxter Peritoneal Dialysis Transfer Sets Recalled for Chemical Exposure
Baxter Healthcare Corporation is recalling 1,240 units of MiniCap Extended Life PD Transfer Sets (Part Number T5C4484) due to potential exposure to polychlorinated biphenyls and related compounds when used in peritoneal dialysis treatments.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp EX Short, Part Number T5C4484; use in Peritoneal Dialysis
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0379-2025·2024-11-27
Baxter MiniCap Dialysis Transfer Sets Recalled for PCB Exposure Risk
Baxter is recalling MiniCap Extended Life PD Transfer Sets used in peritoneal dialysis due to potential exposure to polychlorinated biphenyls (PCBs). About 62,394 units distributed worldwide may be affected.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4483; use in Peritoneal Dialysis
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·24V897000·2024-11-27
Jeep Grand Cherokee side airbags may not deploy in a crash
Chrysler is recalling certain 2022-2024 Grand Cherokee and 2021-2024 Grand Cherokee L vehicles because an improperly secured connector may prevent the front seat side airbags deploying. All units have been remedied.
Product
JEEP — JEEP GRAND CHEROKEE L, GRAND CHEROKEE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V899000·2024-11-27
Keystone Recalls 2025 Arcadia and Cougar Trailers for Hitch Fastener Issue
Keystone is recalling 2025 Arcadia and Cougar trailers because improperly tightened pin box fasteners may loosen, allowing the trailer to detach and increasing crash risk.
Product
KEYSTONE — KEYSTONE COUGAR, ARCADIA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V896000·2024-11-27
Chrysler Recalls 2017-2018 Ram Trucks Due to Brake Control Unit Failure
Chrysler is recalling 2017-2018 Ram 2500, 3500, 4500, and 5500 trucks because the hydraulic control unit may fail, disabling anti-lock brakes and stability controls.
Product
RAM — RAM 5500, 2500, 4500, 3500
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V900000·2024-11-27
Honda Passport and Pilot fuel filler pipes can separate and leak
Honda is recalling certain 2023-2024 Passport and 2023-2025 Pilot vehicles because the fuel filler neck tube and fuel filler pipe may separate, allowing fuel to leak.
Product
HONDA — HONDA PILOT, PASSPORT
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0378-2025·2024-11-27
Baxter MiniCap Peritoneal Dialysis Transfer Set recalled for potential PCB exposure
Baxter Healthcare is recalling 58,680 units of its MiniCap Extended Life PD Transfer Set due to potential exposure to polychlorinated biphenyls (PCBs). Users should stop using affected units and consult their healthcare provider.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4482E; use in Peritoneal Dialysis
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0377-2025·2024-11-27
Baxter Peritoneal Dialysis Transfer Set Recalled for PCB Contamination Risk
Baxter Healthcare is recalling the MiniCap Extended Life PD Transfer Set due to potential exposure to polychlorinated biphenyls (PCBs). Approximately 410,862 units are affected.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4482; use in Peritoneal Dialysis
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0482-2025·2024-11-27
Medical Device Recall: Counterfeit Batteries in Plum Infusion Systems
Counterfeit CSB batteries are being used in Plum Infusion Systems. These unauthorized batteries fail to hold their charge and have not been tested for use with the pumps.
Product
Allegedly counterfeit batteries manufactured by CSB batteries being used with Plum Infusion Systems: Plum 360" Infusion System, Pump List Number 30010; Plum A+ & Plum A+3" Infusion Systems, Pump List Numbers: 11005, 11971, 12391, 12618, 20678, 20679, 20792, 60529, 12348, 1197
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0373-2025·2024-11-27
Peritoneal Dialysis Transfer Set Recalled for PCB Contamination Risk
Baxter Healthcare recalls peritoneal dialysis transfer sets (Part Number 5C4482) due to potential contamination with polychlorinated biphenyls (PCBs). The recall affects 2.7 million units distributed worldwide.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482; use in Peritoneal Dialysis
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0375-2025·2024-11-27
Baxter peritoneal dialysis transfer set recalled for PCB exposure risk
Baxter MiniCap Extended Life PD Transfer Sets (Part 5C4482S) are being recalled due to potential exposure to polychlorinated biphenyls (PCBs). The FDA Class I recall affects 151,020 units distributed worldwide.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482S; use in Peritoneal Dialysis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0140-2025·2024-11-27
Great Value Cheese Danish Recalled for Plastic Pieces
Great Value Cheese Danish is being recalled due to plastic pieces found in the product. Consumers who purchased this item should discard it.
Product
Great Value Cheese Danish 16.5 oz UPC 078742201177, 12 retail units per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0473-2025·2024-11-27
Posi-Stop Injection Needles recalled for manufacturing debris blockage
Hobbs Medical is recalling Posi-Stop Injection Needles due to manufacturing debris that can block needle flow. Some units may contain debris in the inner sheath that prevents injection solutions from functioning properly.
Product
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4704
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0060-2025·2024-11-27
Docusate Sodium 250 mg softgels recalled due to defective blister packaging
Safecor Health is recalling Docusate Sodium 250 mg softgels due to manufacturing defects where blister card-foils separated from the medication cavity, potentially compromising product integrity.
Product
Docusate Sodium 250 mg, 1 Softgel in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-101-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0052-2025·2024-11-27
FDA recalls Ramipril 2.5 mg capsules for manufacturing control deviations
Lupin Pharmaceuticals is recalling Ramipril 2.5 mg capsules after sourcing the active ingredient from an unapproved vendor. Approximately 112,770 bottles were distributed to wholesalers nationwide.
Product
RAMIPRIL — RAMIPRIL (RAMIPRIL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0467-2025·2024-11-27
Bard Marquee Biopsy Instruments Recalled for Potential Needle Detachment
Bard Peripheral Vascular Inc. is recalling Bard Marquee Disposable Core Biopsy Instrument Kits due to a manufacturing defect where some units lack a needle retention feature, risking detachment during use and potential tissue damage or bleeding.
Product
Bard Marquee Disposable Core Biopsy Instrument Kit: BARD MARQUEE KIT 12G X 10 CM, REF: MQK1210; BARD MARQUEE 12G X 10 CM, REF: MQ1210; BARD MARQUEE Kit 12G X 13 CM, REF: MQK1213; BARD MARQUEE 12G X 13 CM, REF: MQ1213
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0055-2025·2024-11-27
Prescription Dextroamphetamine Patches Recalled for Defective Adhesive System
Noven Pharmaceuticals Inc is recalling 685 boxes of XELSTRYM (dextroamphetamine) transdermal patches nationwide due to a defect in the adhesive delivery system. The product does not meet manufacturing specifications.
Product
XELSTRYM — XELSTRYM (DEXTROAMPHETAMINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0051-2025·2024-11-27
Bevacizumab injection syringes recalled for lack of sterility assurance
27,560 bevacizumab injection syringes distributed nationwide are being recalled due to failure to maintain sterility assurance. The affected syringes may not be sterile.
Product
BEVACIZUMAB (AVASTIN)1.25mg/0.05mL, Sterile Injection, 0.5 mL Single-Dose Syringe, Rx Only, Repackaged by: Medivant Healthcare: 24416 N 19th Ave, Phoenix, AZ, NDC 81483-0041-1
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0488-2025·2024-11-27
EnChroma Safety Glasses recalled for defective impact protection
EnChroma Inc recalls 53 units of safety glasses with Rx indoor lenses that fail impact safety standards, posing a risk of eye injury. Affected models include Martinez Cx1 Indoor Rx, Summit Indoor Rx, and Martinez Black Cx Rx.
Product
EnChroma Safety Glasses with Rx Indoor Universal Lenses: Martinez Cx1 Indoor Rx, SKU: Cx.PC.IN.MTZ.BK.Rx; Summit Indoor Rx, Cx.PC.IN.SUM.BK.Rx; Martinez Black Cx Rx, Cx-3.PC.PT.MTZ.BK.Rx
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0141-2025·2024-11-27
Great Value Cinnamon Rolls Recalled for Plastic Contamination Nationwide
The JM Smucker Company is recalling Great Value Cinnamon Rolls nationwide due to possible plastic pieces in the product. Consumers should not consume affected units.
Product
Great Value Cinnamon Rolls 16.5oz UPC 078742201160, 12 retail units per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0477-2025·2024-11-27
JuggerLoc/ToggleLoc 2.9mm Drill Guide Warping in Packaging
Biomet's JuggerLoc/ToggleLoc 2.9mm Drill Guide may warp when removed from packaging, potentially extending surgical time or causing tissue damage requiring intervention.
Product
JuggerLoc/ToggleLoc 2.9mm Drill Guide, Model number 110027357
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0472-2025·2024-11-27
Posi-Stop Injection Needle Recalled Due to Manufacturing Debris Blockage
Hobbs Medical is recalling Posi-Stop Injection Needles (23 Gauge, Lot H11-23-057) because some units contain manufacturing debris that blocks the needle opening, preventing injection solutions from flowing properly.
Product
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4721
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0475-2025·2024-11-27
Posi-Stop 25-Gauge Injection Needles Recalled for Manufacturing Debris Blockage
Hobbs Medical is recalling Posi-Stop 25-Gauge injection needles because some units contain manufacturing debris that blocks the needle's inner diameter, preventing injection solutions from flowing properly.
Product
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4722
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0481-2025·2024-11-27
CAIRE FreeStyle Comfort portable oxygen concentrator battery recharge failure
Caire Inc. is recalling 26 CAIRE FreeStyle Comfort portable oxygen concentrators due to potential battery recharge failure. Affected units identified by serial number may not charge properly.
Product
CAIRE FreeStyle Comfort portable oxygen concentrator, model #AS200-2.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0497-2025·2024-11-27
Philips Vue PACS Diagnostic Viewer Software Recall for Calculation Errors
Philips is recalling Vue PACS Diagnostic Viewer software versions 12.1.5 to 12.2.8.454 because a defect may cause incorrect ischemic map calculations, potentially leading to misdiagnosis.
Product
Vue PACS Diagnostic Viewer with Vue PACS client 12.1.5 to 12.2.8.454 software Model Number: 1149418 Intended use is to provide completely scalable local and wide area PACS (Picture Archiving and Communication System) solutions for hospital and related institutions/sites.
Category
Medical Device
Distribution
Distributed nationwide