State

North Carolina product recalls

72,986 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 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7501–7525 of 83247

SevereFDA (Devices)·Z-1496-2025·2025-04-09
Anesthesia Circuit Kit Flex 2 recalled due to breathing hose crack risk
Draeger's Anesthesia Circuit Kit Flex 2 is recalled because of the potential for cracks to form in the breathing circuit hose. No injuries have been reported.
Product
Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 2 Model/Catalog Number: MP02738 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1494-2025·2025-04-09
Draeger ID Circuit Flex 220 breathing circuit hoses subject to cracking
Draeger's ID Circuit Flex 220 breathing circuit for anesthesia machines may develop cracks in the hose. The recall affects 3,325 units distributed nationwide and internationally.
Product
Brand Name: ID Circuit Product Name: ID Circuit Flex 220 Model/Catalog Number: MP01347 Software Version: Not applicable Product Description: Breathing circuit for conveying breathing gases between an anesthesia machine or ventilator and adult Component: Not applicable
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1497-2025·2025-04-09
Anesthesia Circuit Kit Flex 6 Recalled for Potential Breathing Hose Cracks
Draeger, Inc. is recalling the Anesthesia Circuit Kit Flex 6 (Model MP02744) due to potential cracks forming in the breathing circuit hose. Approximately 293,660 units were distributed nationwide and internationally.
Product
Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 6 Model/Catalog Number: MP02744 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·25V216000·2025-04-09
McLaren brake lines may be routed to the wrong side
McLaren is recalling certain 2020-2025 vehicles because brake lines may be routed incorrectly, activating the brakes on the wrong side and possibly locking a rear wheel.
Product
MCLAREN — MCLAREN GTS, 600LT, 720S SPIDER, ARTURA
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1498-2025·2025-04-09
Anesthesia Circuit Kit Flex (P)2 recalled for potential breathing hose cracks
Draeger, Inc. is recalling the Anesthesia Circuit Kit Flex (P)2 due to the potential for cracks to form in the breathing circuit hose. This FDA Class I recall affects approximately 9,250 units distributed domestically and internationally.
Product
Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex (P)2 Model/Catalog Number: MP02752 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is inten
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1495-2025·2025-04-09
Draeger Anesthesia Circuit Kit Flex 1 recalled for potential hose cracks
Draeger, Inc. is recalling Anesthesia Circuit Kit Flex 1 devices nationwide and internationally due to potential cracks in the breathing circuit hose that conducts anesthesia gases.
Product
Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 1 Model/Catalog Number: MP02737 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1493-2025·2025-04-09
VentStar Flex 220 Breathing Circuit Recalled for Potential Hose Cracks
Draeger, Inc. is recalling 65,150 units of the VentStar Flex 220 breathing circuit due to the potential for cracks to form in the hose. A crack could affect gas delivery during anesthesia or ventilation procedures.
Product
Brand Name: VentStar Product Name: VentStar Flex 220 Model/Catalog Number: MP00355 Software Version: Not applicable Product Description: Breathing circuit for conveying breathing gases between an anesthesia machine or ventilator and adult patients. The breathing circuit is in
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0684-2025·2025-04-09
SeaBear Salmon Chowder Recalled for Potential Seal Failure and Botulinum Risk
SeaBear Smokedhouse Salmon Chowder is recalled due to potential seal failure that could allow Clostridium botulinum contamination. The recall affects 11,152 pouches distributed nationwide.
Product
SeaBear Smokedhouse Salmon Chowder is packaged in flexible retort pouch, net wt. 12-oz., UPC 0 34507 07001 3. Case label: Item 60077 Salmon Chowder 12/12oz, SeaBear/G&D Anacortes, WA.
Category
Food
Distribution
Distributed nationwide
HighNHTSA·25E025000·2025-04-09
Hiab Recalls Waltco ZS-MK2 Lift Gates Due to Pin Seizure Risk
Hiab USA Inc. is recalling specific Waltco ZS-MK2 series lift gates because insufficient lubrication may cause the cylinder pin to seize, leading to lift gate failure and injury risk.
Product
STRUCTURE:BODY:HATCHBACK/LIFTGATE recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1509-2025·2025-04-09
BD Connecta Stopcocks Recalled for Non-U.S. Instructions Shipped to U.S. Market
BD Connecta Luer-Lok 360 stopcocks were distributed with non-U.S. instructions for use. Healthcare facilities should verify they have the correct U.S. instructions before using affected lot numbers.
Product
BD Connecta BD Luer-Lok 360, REF 394910 UDI-DI code: 00382903949106 Connecta¿ Plus 1 and Connecta¿ Plus 3 2-way and 3-way Stopcocks are control valves for use in IV. therapy and hemodynamic pressure monitoring.
Category
Medical Device
Distribution
35 states
HighFDA (Devices)·Z-1481-2025·2025-04-09
Nasopore Nasal Dressings Recalled Due to Breached Sterility Seals
Stryker Corporation is recalling Nasopore nasal dressings due to potential breaches in packaging sterility seals that could compromise product sterilization. Approximately 182,344 units have been distributed nationwide.
Product
Nasopore 4cm Standard 2PK fragmentable nasal dressing, Catalog Number 5400-212-004S and Nasopore 4cm Firm 2PK Catalog Number 5400-222-004S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1516-2025·2025-04-09
Surgical Suture Recall Due to Silicone Curing Defect
Ethicon Endo Surgery recalls ETHIBOND EXCEL surgical sutures worldwide due to curing issues with the silicone coating on the needles identified during manufacturing.
Product
ETHIBOND EXCEL GRN 36IN(90CM) USP2-0(M3) D/A MH
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0306-2025·2025-04-09
Biocon Pharma atorvastatin calcium tablets recalled for failed dissolution specifications
Biocon Pharma is recalling 2,184 bottles of Atorvastatin Calcium Tablets USP 40 mg nationwide. The product failed to meet required dissolution specifications, which may affect medication absorption.
Product
ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1515-2025·2025-04-09
Ethicon PROLENE BLU Surgical Sutures Recalled for Manufacturing Defect
Ethicon is recalling specific lots of PROLENE BLU surgical sutures due to silicone curing issues during needle manufacturing.
Product
PROLENE BLU 18IN(45CM) USP6-0(M0.7) S/A P-1 PRM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1517-2025·2025-04-09
Clinical Chemistry Analyzer Recalled for Software Defect in Test Result Calculation
Beckman Coulter is recalling certain DxC 500 AU Clinical Chemistry Analyzers due to a software defect that prevents calculated test results from being recalculated when constituent tests are rerun, potentially delaying patient result reporting.
Product
DxC 500 AU Clinical Chemistry Analyzer, Catalog Numbers/UDI codes: C63519 / 14987666545058 C63520 / 14987666545065 The Beckman Coulter DxC 500 AU Clinical Chemistry Analyzer is an automated chemistry analyzer that measures analytes in samples, in combination with appropriate
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0681-2025·2025-04-09
Lean Cuisine Lemon Garlic Shrimp Stir Fry Recalled Due to Foreign Material
Nestle-USA recalls Lean Cuisine Lemon Garlic Shrimp Stir Fry (10 oz) due to potential wood-like foreign material. Approximately 7,212 cases distributed across 37 states; check Batch Number 4214595511 (Best By September 2025).
Product
Lean Cuisine Lemon Garlic Shrimp Stir Fry, NET WT 10 OZ (283g), in a plastic tray with film seal, packaged inside a paperboard carton; 10 consumer units per case
Category
Food
Distribution
37 states
HighFDA (Devices)·Z-1470-2025·2025-04-09
Nasopore nasal dressing may have compromised sterile packaging
Stryker is recalling Nasopore Standard 4cm nasal dressings because the blister seals may develop bubbles, potentially compromising the sterility barrier. Affected units should not be used.
Product
Nasopore Standard 4cm fragmentable nasal dressing, Catalog Numbers 5400-010-004 and 5400-010-004ITL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1480-2025·2025-04-09
Nasopore Nasal Dressing Recall Due to Compromised Sterile Packaging Seals
Stryker Corporation is recalling Nasopore nasal dressings due to potentially compromised sterile packaging seals. Affected units totaling 182,344 may have lost sterility, posing a contamination risk.
Product
Nasopore 4cm Standard 2PK fragmentable nasal dressing, Catalog Number 5400-212-004S and Nasopore 4cm Firm 2PK Catalog Number 5400-222-004S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0685-2025·2025-04-09
SeaBear Clam Chowder Recalled for Potential Botulinum Contamination
SeaBear Smokedhouse Alehouse Clam Chowder pouches are recalled nationwide due to potential seal failure that could allow Clostridium botulinum contamination. Consumers should not consume the product.
Product
SeaBear Smokedhouse Alehouse Clam Chowder is packaged in retort pouch, net wt. 12-oz., UPC 0 34507 07021 1. Case label, item 60104, Alehouse Chowder 12/CS.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1482-2025·2025-04-09
Stryker nasal wound dressing recalled for defective sterile packaging seal
Stryker Corporation is recalling 182,344 units of Hemopore 2PK nasal/sinus wound dressing due to potential bubbles in blister seals that indicate sterility breach. Affected lot numbers are 2024020221, 2024051720, and 2024082321.
Product
Hemopore 2PK nasal/sinus temporary wound dressing, Catalog Number 5400-222-208S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0693-2025·2025-04-09
Good & Gather Baby Vegetable Puree Recalled for Elevated Lead Levels
Good & Gather baby vegetable puree (4 oz) is being recalled due to elevated levels of lead. The recall affects 25,600 units distributed nationwide by Target.
Product
Good & Gather baby Pea, Zucchini, Kale & Thyme Vegetable Puree. Net Wt 4 oz. (113g). 6+ months. UPC 1 91907-99314 1. Distributed by Target Corporation, Minneapolis, MN 55403. Product of Colombia
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1506-2025·2025-04-09
Medtronic A820 myPTM Infusion Pump Software Shows Delayed Patient Response
Medtronic is recalling the A820 myPTM Software Application used with SynchroMed infusion pumps because the app is taking longer than expected to respond to patient interactions. Approximately 4365 units are affected worldwide.
Product
A820 myPTM Software Application associated with Medtronic SynchroMed Pump and Infusion System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0682-2025·2025-04-09
Lean Cuisine Butternut Squash Ravioli Recalled for Potential Foreign Material
Nestle-USA recalls Lean Cuisine Butternut Squash Ravioli for potential wood-like foreign material. Approximately 50,611 cases distributed across 36 states are affected.
Product
Lean Cuisine Butternut Squash Ravioli, NET WT 9 7/8 OZ (280g), in a plastic tray with film seal, packaged inside a paperboard carton; packed 12 consumer units per case
Category
Food
Distribution
37 states
HighFDA (Devices)·Z-1474-2025·2025-04-09
Nasopore nasal dressing recall: compromised sterile barrier seals
Stryker recalls Nasopore 4cm fragmentable nasal dressings due to potential blister seal damage that compromises the sterile barrier. Nationwide distribution affected.
Product
Nasopore 4cm fragmentable nasal dressing, Firm Catalog Number 5400-020-004 and Forte Catalog Number 5400-020-004ITL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1501-2025·2025-04-09
Phoroptor VRx Digital Refraction System Recalled for Detachable Head
Reichert is recalling 1,876 units of the Phoroptor VRx Digital Refraction System (Model 16242) due to an assembly defect that could cause the refraction head to detach during eye examinations.
Product
Phoroptor VRx Digital Refraction System Model Numbers: 16242
Category
Medical Device
Distribution
Distributed nationwide