State

North Carolina product recalls

72,940 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 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3776–3800 of 83201

HighFDA (Drugs)·D-0263-2026·2026-01-21
Alka Seltzer recalled over insanitary conditions at a distribution center
Gold Star Distribution is recalling Alka Seltzer over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.
Product
Alka Seltzer, a) Original, 2 tablets per packet in 58 count box, UPC: 815556020033, 016500514473, b) Plus Cold & Flu, 2 tablets per packet in 36 count box, UPC: 016500594932
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1062-2026·2026-01-21
Allura Xper FD10C systems recalled over a missing cooling unit drip tray
Philips Medical Systems Nederland is recalling 38 Allura Xper FD10C systems because the drip tray beneath the cooling unit may not have been installed.
Product
Product Name: Allura Xper FD10C; Model number: 722001;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1075-2026·2026-01-21
Allura Xper FD20, model 722028, recalled over a missing drip tray
Philips Medical Systems Nederland is recalling 2 Allura Xper FD20 systems because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD20; Model Number: 722028;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1053-2026·2026-01-21
Donor nephrectomy accessory kits recalled over recalled B. Braun sets
Medline is recalling 33 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Product
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: RR-LAP DONOR NEP ACCESSORY, Medline kit SKU DYNJ63395B
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1056-2026·2026-01-21
IV start kits recalled over recalled B. Braun administration sets inside
Medline is recalling 5314 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Product
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) IV START KIT NS, Medline kit SKU DYKM1980C; 2) (134) L&D IV-START SET, Medline kit SKU DYKM2137B; 3) IV START KIT, Medline kit SKU DYKS1372C; 4) IV START KIT, Medline kit
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0274-2026·2026-01-21
Admission and admin kits recalled over recalled B. Braun administration sets
Medline is recalling 1725 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Product
CHILDREN NYQUIL, COLD&FLU, BERRY, 8oz, 12ct
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0259-2026·2026-01-21
Carotid anesthesia kits recalled over recalled B. Braun administration sets inside
Medline is recalling 10 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1091-2026·2026-01-21
Azurion systems recalled over six identified software issues
Philips Medical Systems Nederland is recalling 10,466 Azurion systems on software versions R2.1.10 and R2.2.10 over six identified software issues including continuous restart.
Product
Philips Azurion Systems with software versions R2.1.10 and R2.2.10. Includes the following label descriptions and corresponding models: 1. Azurion 3 M12. Model Numbers: 722063, 722221. 2. Azurion 3 M15. Model Numbers: 722064, 722222, 722280. 3. Azurion 5 M12. Model Num
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1043-2026·2026-01-21
Neurostimulator clinician programmer app recalled over faults during device use
Medtronic is recalling 7,123 units of the Vanta Clinician Programmer Application after complaints that it does not function as intended during use.
Product
A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and 2.0.2683, Product number A71200. Software is deployed and operated on Samsung tablets (CFN CT900).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0280-2026·2026-01-21
PALACOS MV plus G bone cement recalled because ampoules may not break
Heraeus Medical is recalling PALACOS MV+G pro 40 and PALACOS MV+G pro 80 bone cement because an unfortunate combination of factors can leave ampoules unbroken, so no appropriate cement dough is formed.
Product
Swan, White Clear Alcohol, 50%, 16oz, 12 count
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1051-2026·2026-01-21
Pre-op kits recalled because they contain recalled B. Braun administration sets
Medline is recalling 32 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Product
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) DELUXE PRE OP KIT, Medline SKU DYKS2034A; 2) DELUXE PRE OP KIT, Medline SKU DYKS2006B.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1049-2026·2026-01-21
Allura Xper FD20/10 systems recalled over a missing cooling unit drip tray
Philips Medical Systems Nederland is recalling 4 units of the Allura Xper FD20/10, model 722029, because the drip tray beneath the cooling unit may not have been installed.
Product
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: AN01 CAROTID ANESTH KIT-LF, Medline Kit SKU PHS972096014B
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1038-2026·2026-01-21
Universal implant inserters recalled because the rotation tool handle can untread
Medicrea International is recalling 44 IB3D Universal Implant Inserters because, following complaints, the orthopedic rotation tool handle may untread from the shaft.
Product
Medicrea, IB3D Universal Implant Inserter, Rx Only REF: A24000000
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1072-2026·2026-01-21
Allura Xper FD20 OR Table recalled over a missing cooling unit drip tray
Philips Medical Systems Nederland is recalling 4 units of the Allura Xper FD20 OR Table, model 722023, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD20 OR Table; Model Number: 722023;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1076-2026·2026-01-21
Preoperative kits recalled over recalled B. Braun administration sets inside
Medline is recalling 11173 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Product
Allura Xper FD20/10; Model Number: 722029;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1069-2026·2026-01-21
Allura Xper FD10/10, model 722011, recalled over a missing drip tray
Philips Medical Systems Nederland is recalling 21 units of the Allura Xper FD10/10, model 722011, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD10/10; Model Number: 722011;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1086-2026·2026-01-21
Laparoscopy kits recalled over suction irrigators that can leak during use
Medline is recalling 41,432 laparoscopy convenience kits containing Stryker Strykeflow 2 Suction Irrigators, which can leak or emit vaporized saline during use.
Product
Medline medical procedure convenience kits labeled as: 1) LAPAROSCOPY CDS-LF, REF CDS860235L; 2) GENERAL LAPAROSCOPIC, REF CDS930223M; 3) LAP CHOLE CDS, REF CDS983678K; 4) LAPAROSCOPY PELV CDS, REF CDS983679K; 5) LAP CHOLE CDS-LF, REF CDS983752M; 6) LAP CHOLE CDS-LF,
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1067-2026·2026-01-21
Allura Xper FD20 Biplane systems recalled over a missing cooling unit drip tray
Philips Medical Systems Nederland is recalling 18 units of the Allura Xper FD20 Biplane, model 722008, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD20 Biplane; Model Number: 722008;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1090-2026·2026-01-21
Robotic prostate kits recalled over suction irrigators that can leak
Medline is recalling 12 units of procedure convenience kits containing Stryker Strykeflow 2 Suction Irrigators, which can leak or emit vaporized saline during use.
Product
Medline medical procedure convenience kits labeled as: KIT ROBOTICS UROLOGY PROSTATE, REF DYKMBNDL116G
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1039-2026·2026-01-21
Spinal instrument sets recalled because the rotation tool handle can untread
Medicrea International is recalling 44 IB3D PL Instruments Sets because, following complaints, the orthopedic rotation tool handle may untread from the shaft.
Product
Medicrea, IB3D PL Instruments Set, Rx Only REF: SPS03174
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1070-2026·2026-01-21
Surgical procedure packs recalled over recalled B. Braun administration sets inside
Medline is recalling 338 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.
Product
Allura Xper FD20; Model Number: 722012;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1068-2026·2026-01-21
Allura Xper FD10, model 722026, recalled over a missing cooling unit drip tray
Philips Medical Systems Nederland is recalling 95 units of the Allura Xper FD10, model 722026, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD10; Model Number: 722010;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1065-2026·2026-01-21
Allura Xper FD10/10, model 722005, recalled over a missing drip tray
Philips Medical Systems Nederland is recalling 14 units of the Allura Xper FD10/10, model 722005, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD10/10; Model Number: 722005;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1064-2026·2026-01-21
Allura Xper FD10, model 722003, recalled over a missing drip tray
Philips Medical Systems Nederland is recalling 93 units of the Allura Xper FD10, model 722003, because the drip tray beneath the cooling unit may not have been installed.
Product
Allura Xper FD10; Model Number: 722003;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1087-2026·2026-01-21
PALACOS MV bone cement recalled because ampoules may not break
Heraeus Medical is recalling PALACOS MV pro 40 and PALACOS MV pro 80 bone cement because an unfortunate combination of factors can leave ampoules unbroken, so no appropriate cement dough is formed.
Product
Medline medical procedure convenience kits labeled as: 1) WCH BARI-GASTRECTOMY CDS, REF CDS860237AF; 2) ROBOTIC PROCEDURE, REF CDS982128Q; 3) CUH THORACIC, REF CDS984338M; 4) THORACIC PROCEDURE, REF CDS984640I; 5) DAVINCI ROBOTIC PACK-LF, REF DYNJ0525321O; 6) LAP CHO
Category
Medical Device
Distribution
Distributed nationwide