State

California product recalls

73,106 recalls have nationwide distribution and so reach California. 13,252 additional recalls listed California specifically in their distribution scope.

What the numbers show

Total: 13,252
Critical: 1,605
Severe: 2,847
Most recent: 2026-10-02

Of the 13,252 recalls naming California we have scored against our rubric, 1,605 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,847 (21%) are Severe.

Which agencies issued them

These figures cover only the 13,252 recalls whose distribution notice names California specifically. The 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

12101–12125 of 86358

HighFDA (Devices)·Z-2176-2024·2024-07-03
VASOVIEW HemoPro harvesting system fluid ingress may disable cautery
Maquet Cardiovascular recalls VASOVIEW HemoPro Endoscopic Vessel Harvesting Systems due to fluid ingress into the harvesting tool handle, which may prevent necessary cautery or cause unintended cautery during surgical procedures.
Product
The VASOVIEW HemoPro Endoscopic Vessel Harvesting Systems are designed for use in conjunction with the 7 mm Extended Length Endoscope. The Harvesting Cannula has four lumens which house the Endoscope, C-Ring, distal lens washer tube, and harvesting tool for cutting and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2185-2024·2024-07-03
AXIOM Vertix Solitaire Medical Imaging Device Recall: Fire Risk from Power Supply Defect
Siemens is recalling 4 AXIOM Vertix Solitaire medical imaging devices due to a short circuit in the touch display power supply that may cause overheating and fire. Units with serial numbers 1004, 1006, 1011, and 1014 are affected.
Product
AXIOM Vertix Solitaire - The Vertix MD Trauma has been specially designed for examining emergency and accident patients as well as for use in outpatient departments. Material Number: 8627718
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2201-2024·2024-07-03
Medtronic MIRRO MRI implantable defibrillator recalled for weld defect
Medtronic is recalling 3 MIRRO MRI DR SureScan implantable cardioverter defibrillators due to a manufacturing weld crack that caused devices to fail quality checks. The defect was detected during manufacturing before devices reached patients.
Product
MIRRO MRI DR SureScan, Model Number DDME3D1, Implantable Cardioverter Defibrillator
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·24289·2024-07-03
SWOMOG Children's Two-Piece Pajama Sets Recalled for Burn Hazard
SWOMOG children's two-piece pajama sets sold on Amazon.com from May 2022 through January 2024 violate federal flammability standards for children's sleepwear, posing a burn hazard. Consumers should stop use immediately and contact SWOMOG for a full refund.
Product
SWOMOG Children's Two-Piece Pajama Sets
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2221-2024·2024-07-03
Endoscopic Kittner Surgical Instrument Recalled for Sterile Barrier Defect
ASPEN SURGICAL is recalling 1,900 units of the Endoscopic Kittner Blunt Dissecting Instrument (Model KT-9101) due to a potential defect in the sterile barrier seal.
Product
Endoscopic Kittner Blunt Dissecting Instrument, Intended to be used for blunt dissection of tissue, Model Number KT-9101
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·24V506000·2024-07-03
Motorhomes recalled for missing spare tire wheel bolts
Tiffin is recalling certain motorhomes because the wheel bolts for the spare tire may be missing. A spare tire without correct bolts could detach and increase crash risk.
Product
TIFFIN — TIFFIN CONVOY, CAHABA, GH1
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2219-2024·2024-07-03
Stryker Hoffman LRF Wire Tensioner Adjustment Ring May Become Loose
Stryker is recalling 39 Hoffman LRF Wire Tensioner devices because the adjustment ring may loosen, preventing proper tension setting. No injuries reported.
Product
Stryker Hoffman LRF Wire Tensioner REF 4933-9-100, a component of the Hoffmann LRF System.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·24E056000·2024-07-03
Reyco Granning Recalls Independent Front Suspension Assemblies Due to Brittle Bolts
Reyco Granning is recalling specific independent front suspension assemblies because lower control arm retention bolts may become brittle and break, posing an injury risk.
Product
SUSPENSION:FRONT:CONTROL ARM:LOWER ARM recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2218-2024·2024-07-03
Prelude Roadster Guide Sheaths Recalled Due to Instruction Defect
Merit Medical Systems is recalling Prelude Roadster Guide Sheaths due to an instructional defect. Older instructions directing tight connection assembly may cause over-tightening, leading to swivel nut detachment.
Product
Prelude Roadster Guide Sheath REF: -PG4F45S -PG4F90S -PG5F45MP -PG5F45R -PG5F45S -PG5F45S018 -PG5F90MP -PG5F90S -PG5F90S018 -PG6F45HS -PG6F45MP -PG6F45R -PG6F45S -PG6F45S018 -PG6F65MP -PG6F65S -PG6F65SX -PG6F90MP -PG6F90MPX -PG6F90SX -PG6F90SX018 -PG7F45MP…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·24V511000·2024-07-03
Freightliner Custom Chassis S2C and S2RV Brake Light Recall
Daimler Trucks North America is recalling 2023-2025 Freightliner Custom Chassis S2C and S2RV trucks because brake lights may not illuminate during active brake assist events.
Product
FCCC — FCCC S2C, S2RV
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-1426-2024·2024-07-03
Chocolate Chunk Cookie Mix Recalled for Undeclared Coconut Allergen
Penguin Natural Foods is recalling 'THE PERFECT CHOCOLATE CHUNK COOKIE MIX Cravings by Chrissy Teigen' because the product contains undeclared coconut. Consumers with coconut allergies face a serious health risk.
Product
"THE PERFECT CHOCOLATE CHUNK COOKIE MIX Cravings by Chrissy Teigen NET WT. 15.76 OZ (447g)" Packaged in a beige cardboard box, with green lettering
Category
Food
Distribution
6 states
HighFDA (Devices)·Z-2186-2024·2024-07-03
Siemens Multix TOP X-ray Table Recalled Due to Fire Risk
Siemens is recalling 3 Multix TOP I PRO radiographic X-ray tables due to a short circuit in the Touch Display power supply unit that may cause overheating and fire.
Product
MULTIX TOP - Intended Use: The Multix TOP I PRO Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number:475517
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1423-2024·2024-07-03
Fresh Catch Inc. Yellowfin Tuna Recalled for High Histamine Levels
Fresh Catch Inc. is recalling Yellowfin Tuna for high histamine levels. No illnesses have been reported.
Product
Fresh Catch Inc. Yellowfin Tuna, 1 loin per case packaged in carboard boxes with keep refrigerated label
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-2190-2024·2024-07-03
Medtronic Implantable Cardioverter Defibrillator Recalled for Manufacturing Weld Defect
Medtronic recalled 14 COBALT HF QUAD CRT-D MRI SureScan implantable defibrillators due to a weld crack manufacturing defect detected during quality control testing.
Product
COBALT HF QUAD CRT-D MRI SureScan, Model Number DTPB2QQ, Implantable Cardioverter Defibrillator
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2211-2024·2024-07-03
Medtronic ICD Implants Recalled for Manufacturing Weld Crack Defects
Medtronic recalls 9 units of CROME VR MRI SureScan implantable cardioverter defibrillators due to a manufacturing weld crack that caused devices to fail quality control leak testing.
Product
CROME VR MRI SureScan, Model Number DVPC3D1, Implantable Cardioverter Defibrillator
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2202-2024·2024-07-03
Implantable Cardioverter Defibrillator Recalled Due to Manufacturing Weld Defect
Medtronic is recalling 26 MIRRO MRI DR SureScan Implantable Cardioverter Defibrillators due to a manufacturing defect involving a weld crack that could affect device function.
Product
MIRRO MRI DR SureScan, Model Number DDME3D4, Implantable Cardioverter Defibrillator
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2175-2024·2024-07-03
Endoscopic Vessel Harvesting System Recalled Due to Potential Cautery Malfunction
Maquet Cardiovascular recalls VasoView HemoPro 2 vessel harvesting systems due to potential fluid ingress that may prevent or unintentionally activate cautery function. The recall affects 430,037 units distributed worldwide.
Product
The VASOVIEW HemoPro 2 Endoscopic Vessel Harvesting System, labeled as the following: 1. VasoView Hemopro 2, Model Number: VH-4000. 2. VasoView Hemopro 2 with Vasoshield. Model Number: VH-4001. The VASOVIEW HemoPro 2 Endoscopic Vessel Harvesting Systems are designed for use…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1405-2024·2024-07-03
Wakefield Ham, Egg & Cheese Muffins Recalled for Possible Listeria Contamination
Classic Delight LLC is recalling 1,366 cases of Wakefield Ham, Egg & Cheese Muffins due to possible Listeria monocytogenes contamination. The affected products were distributed across 14 states.
Product
(Item 806604) Wakefield Ham, Egg & Cheese Muffin
Category
Food
Distribution
14 states
HighFDA (Drugs)·D-0564-2024·2024-07-03
Buprenorphine Injection Recalled Due to Incomplete Seal Integrity Issue
Pfizer is recalling specific lots of Buprenorphine Hydrochloride Injection due to potential incomplete crimp seals that could compromise product sterility. Patients using affected lots should consult their healthcare provider.
Product
BUPRENORPHINE HYDROCHLORIDE — BUPRENORPHINE HYDROCHLORIDE (BUPRENORPHINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1401-2024·2024-07-03
Wakefield Sausage, Egg & Cheese Biscuits Recalled for Possible Listeria Contamination
Classic Delight LLC is recalling Wakefield Sausage, Egg & Cheese Biscuits (Item 514712) due to possible Listeria monocytogenes contamination. The affected products were distributed in 14 states.
Product
(Item 514712) Wakefield Sausage, Egg & Cheese Biscuit
Category
Food
Distribution
14 states
HighFDA (Food)·F-1411-2024·2024-07-03
Wakefield Chicken and Cheese Kaiser Rolls Recalled for Possible Listeria Contamination
Classic Delight LLC is recalling 1,250 cases of Wakefield Chicken & Cheese Kaiser Rolls due to possible Listeria monocytogenes contamination. The affected products were distributed across 14 states.
Product
(Item 806687) Wakefield Chicken & Cheese Kaiser Roll
Category
Food
Distribution
14 states
HighFDA (Devices)·Z-2208-2024·2024-07-03
Medtronic COBALT VR MRI SureScan implantable defibrillators recalled for manufacturing defect
Medtronic is recalling 4 COBALT VR MRI SureScan implantable cardioverter defibrillators due to a manufacturing defect involving a weld crack identified during quality control testing.
Product
COBALT VR MRI SureScan, Model Number DVPB3D4, Implantable Cardioverter Defibrillator
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1398-2024·2024-07-03
Wakefield Southern Chicken Biscuit recalled for possible Listeria contamination
Classic Delight LLC is recalling Wakefield Southern Chicken Biscuit (Item 176594) due to possible Listeria monocytogenes contamination. The product was distributed in 14 states with multiple affected lot numbers.
Product
(Item 176594) Wakefield Southern Chicken Biscuit
Category
Food
Distribution
14 states
HighFDA (Food)·F-1396-2024·2024-07-03
Classic Delight Breaded Chicken Waffle Recalled for Possible Listeria Contamination
Classic Delight Breaded Chicken Waffle (Item 7626) for institutional use is being recalled due to possible contamination with Listeria monocytogenes. The recall affects 644 cases distributed to institutions in 14 states.
Product
(Item 7626) Classic Delight Breaded Chicken Waffle - INSTITUTIONAL USE ONLY
Category
Food
Distribution
14 states
HighFDA (Devices)·Z-2173-2024·2024-07-03
Sight OLO CBC Test Kit Lot Recalled for Bacterial Contamination
One lot of Sight OLO CBC Test Kit is being recalled due to bacterial contamination that causes artificially elevated platelet counts. The affected kits may produce inaccurate test results.
Product
Sight OLO CBC Test Kit, Model/Catalog Number: TK1. A disposable cartridge and sample preparation tools for use with the Sight OLO CBC analyzer.
Category
Medical Device
Distribution
Distributed nationwide