State

California product recalls

73,198 recalls have nationwide distribution and so reach California. 13,255 additional recalls listed California specifically in their distribution scope.

What the numbers show

Total: 13,255
Critical: 1,605
Severe: 2,847
Most recent: 2026-10-02

Of the 13,255 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 13,255 recalls whose distribution notice names California specifically. The 73,198 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

14001–14025 of 86453

HighFDA (Devices)·Z-1098-2024·2024-03-06
MEDLINE Medical Device Kits Recalled for Potential Sterility Issues
Medline Industries recalls multiple medical device kits and trays manufactured with components that may lack sterility. The affected solutions could be non-sterile, posing a potential safety risk.
Product
MEDLINE Kits, trays, and packs labeled as follows: a) Description, REF DYNDH1679; b) BREAST BIOPSY TRAY, REF DYNDH1664; c) BREAST BIOPSY TRAY, REF DYNDH1431A; d) BREAST BIOPSY TRAY, REF DYNJ46448; e) BREAST BIOPSY TRAY, REF DYKE1520B; f) COLON KIT- BERLIN, REF…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0355-2024·2024-03-06
Omeprazole and Sodium Bicarbonate Prescription Drug Recalled Due to Subpotency
Bausch Health Companies is recalling 3,600 cartons of Omeprazole and Sodium Bicarbonate nationwide. The drug was found to be subpotent, containing less active ingredient than specified.
Product
OMEPRAZOLE AND SODIUM BICARBONATE — OMEPRAZOLE AND SODIUM BICARBONATE (OMEPRAZOLE, SODIUM BICARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1199-2024·2024-03-06
Integra Cranial Access Kit recall over sterile packaging defect
Integra LifeSciences is recalling the Cranial Access Kit due to a defect in the sterile packaging that may compromise product sterility. Affects 30 units distributed worldwide.
Product
Ref No: INS7270 / Integra¿ Cranial Access Kit. For access to the subarachnoid space or the lateral ventricles of the brain.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0931-2024·2024-03-06
Chin Jung White Kimchi Recalled Due to Undeclared Fish Allergen
Chin Jung White Kimchi is being recalled because it contains undeclared fish, a common allergen. Consumers with fish allergies should not consume this product.
Product
Chin Jung White Kimchi - 3 lb. 8 oz (1.58 kg) plastic jars
Category
Food
Distribution
3 states
HighFDA (Food)·F-0932-2024·2024-03-06
Chin Jung White Kimchi Recalled Due to Undeclared Fish Allergen
Chin Jung White Kimchi jars recalled due to undeclared fish allergen. Products distributed to supermarkets in California, Colorado, and Nevada may pose risk to consumers with fish allergies.
Product
Chin Jung White Kimchi - 7 lb. 8 oz.(3.4 kg) plastic jars
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-1197-2024·2024-03-06
Integra Cranial Access Kit Recalled Due to Packaging Integrity Defect
Integra LifeSciences is recalling 188 units of the Integra Cranial Access Kit because defective sterile packaging may have compromised product sterility.
Product
Ref No: INS7250 / Integra Cranial Access Kit. For access to the subarachnoid space or the lateral ventricles of the brain.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0349-2024·2024-03-06
FDA Recalls Fluticasone Propionate Nasal Spray Due to Suspected Bacterial Contamination
The FDA is recalling Fluticasone Propionate Nasal Spray due to suspected potential presence of Burkholderia cepacia complex bacteria. The affected lot (TX5275) was distributed nationwide.
Product
FLUTICASONE PROPIONATE — FLUTICASONE PROPIONATE (FLUTICASONE PROPIONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1203-2024·2024-03-06
Integra Cranial Access Kit Recalled Due to Sterile Packaging Defect
Integra LifeSciences is recalling the Cranial Access Kit due to a defect in sterile packaging that could compromise product sterility. The device is used for neurosurgical access to the brain.
Product
Ref No: INSHITHRZN / Integra Cranial Access Kit. For access to the subarachnoid space or the lateral ventricles of the brain.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0933-2024·2024-03-06
MUTTI Crushed Tomatoes Recall Due to Can Lining Detachment
Mutti USA is recalling MUTTI Crushed Tomatoes because the internal can lining may be detaching into the product. The recall affects 137,634 units distributed to 24 states.
Product
MUTTI Crushed Tomatoes; Polpa; Net Wt 27.9 OZ (1lb 11.9 OZ) 790g; UPC 85469300071
Category
Food
Distribution
25 states
HighFDA (Devices)·Z-1213-2024·2024-03-06
Colonoscope Model PCF-HQ190L Recalled for Missing Protective Adhesive
Olympus is recalling 28 colonoscopes (Model PCF-HQ190L) due to missing adhesive that protects the device from vibration, temperature changes, and physical shock. The defect could cause device malfunction during procedures.
Product
Colonoscope, Model Number PCF-HQ190L.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1217-2024·2024-03-06
Orthopedic knee implant recall due to potential stem misalignment
United Orthopedic Corporation recalls USTAR II knee implants due to potential incorrect orientation of the curved stem. Affected products were distributed across multiple US states and internationally.
Product
USTAR II Knee System : Cemented Curved Stem, RHS Ti Plasma Spray, Reference Numbers: REF: PE25153109 - PE25151109 - 9x125mm, PE25151111 - 11X125, PE25151113 - 13X125mm, PE25151115 - 15X125mm, PE25151117 - 17X125mm, PE25151119 - 19X125mm, PE25151209 - 9X150mm, PE25151211…
Category
Medical Device
Distribution
9 states
HighFDA (Devices)·Z-1215-2024·2024-03-06
Hip Implant System Recalled for Potential Incorrect Stem Orientation
United Orthopedic Corporation is recalling the USTAR II Hip System Press-Fit Curved Stem due to a potential risk that the implant curved stem may be oriented incorrectly. The FDA Class II recall affects 598 units.
Product
USTAR II Hip System Press-Fit Curved Stem, RHS Ti Plasma Spray for the following reference numbers: REF: PE11151211 - 11x150mm, PE11151213 - 13x150mm, PE11151215 - 15x150mm, PE11151217 - 17x150mm, PE11151411 - 11x200mm, PE11151413 - 13x200mm, PE11151415 - 15x200mm…
Category
Medical Device
Distribution
9 states
HighFDA (Devices)·Z-1121-2024·2024-03-06
Medline Nursing Education Kits Recalled for Potential Lack of Sterility
Medline Industries recalls 844 units of nursing education kits and trays due to potential lack of sterility in Nurse Assist irrigation solution components. Products distributed nationwide and internationally.
Product
Medline Kits, trays, and packs labeled as follows: a) NUR 105, REF EDUC05053B; b) NUR 213, REF EDUC05054B; c) NURSING SKILLS, REF EDUC05050B; d) NURSING SUPPLY BAG, REF EDUC1024
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1212-2024·2024-03-06
Olympus colonoscope PCF-H190TL recalled for missing protective adhesive
Olympus has recalled certain repaired colonoscope models lacking protective adhesive that could fail under vibration, temperature, or severe shock loads. Affected models include the PCF-H190TL, distributed nationwide.
Product
Colonoscope, Model Number PCF-H190TL.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1208-2024·2024-03-06
Colonoscope Model CF-Q180AL Recalled Due to Missing Protective Adhesive
Olympus is recalling two colonoscopes (Model CF-Q180AL, serial numbers 2602060 and 2603763) due to missing protective adhesive that normally guards against vibration, temperature changes, and shock loads.
Product
Colonoscope, Model Number CF-Q180AL.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·24V177000·2024-03-06
2022-2024 Triumph Speed Triple motorcycles recalled for engine overheating
Triumph is recalling certain 2022-2024 Speed Triple RS and RR motorcycles because the engine may overheat and cause a coolant leak, increasing injury risk. Dealers will replace the engine software free of charge.
Product
TRIUMPH — TRIUMPH SPEED TRIPLE RS, SPEED TRIPLE RR
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1206-2024·2024-03-06
Colonoscope Model CF-HQ190I recalled for missing protective adhesive
Olympus is recalling certain repaired Model CF-HQ190I colonoscopes assembled without protective adhesive, which may cause equipment failure under vibration, temperature changes, or shock.
Product
Colonoscope, Model Number CF-HQ190I.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0359-2024·2024-03-06
7 Eleven Hand Sanitizer Gel recalled for manufacturing facility deficiencies
Seatex LLC is recalling 1,282 cases of 7 Eleven Hand Sanitizer Gel due to manufacturing facility deficiencies found during FDA inspection. The product was distributed nationwide.
Product
7 Eleven Hand Sanitizer Gel, Ethanol 70% v/v Antiseptic, Mountain Spring Scent, 1250 mL cases, Magnus 16005 Gateway Drive, Ste 300, Frisco, TX 75033
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0361-2024·2024-03-06
Moxifloxacin Ophthalmic Injection Solution Recalled for Glass Particle Contamination
Denver Solutions is recalling Moxifloxacin PF eye injection vials nationwide due to glass delamination in the vials. The affected product is used for eye surgery injections.
Product
Moxifloxacin PF, 1mg/ml, in Sterile Balanced Salt Solution (BSS) Sterile injection, Intracameral Use Only, Single- Dose Vial, Leiters 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-096-42
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0353-2024·2024-03-06
CVS Health Lubricant Eye Ointment recalled due to lack of sterility assurance
CVS Health Lubricant Eye Ointment is being recalled nationwide due to lack of sterility assurance during manufacturing. The recall affects 159,334 units distributed in 3.5-gram tubes with lot numbers A2F03, A2I02, A2L02, A3C04, and A3H04.
Product
CVS Health Lubricant Eye Ointment (Mineral oil 31.9% Emollient, White petrolatum 57.7% Emollient), Packaged in in 3.5 gram tubes, Distributed by: CVS Pharmacy, Inc. One CVS Drive Woonsocket, RI 02895, NDC 76168-707-35, UPC 050428634141
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1218-2024·2024-03-06
Bone plates and surgical screws distributed without FDA pre-market clearance
Acumed LLC is recalling 2,952,121 units of Acu-Loc bone plates, screws, and accessories distributed worldwide because they were placed on the market without FDA pre-market clearance. The safety and effectiveness of these devices have not been verified by the FDA.
Product
Acu-Loc and Acu-Loc 2 bone plates, screws and accessories for the following REF: 70-0045 Acu-Loc VDU Plate Standard, Left; 70-0045-S Acu-Loc VDU Plate Standard, Left; 70-0046 Acu-Loc VDU Plate Standard, Right; 70-0046-S Acu-Loc VDU Plate Standard, Right; 70-0047 Acu-Loc VDU…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1196-2024·2024-03-06
Integra cranial access kit recalled for sterile packaging failure
Integra LifeSciences is recalling 1,324 cranial access kits due to sterile packaging defects that may compromise product sterility.
Product
Ref No: INS5HND / Integra Cranial access kit (without Prep solutions) Bit and Guard. For access to the subarachnoid space or the lateral ventricles of the brain.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1194-2024·2024-03-06
Integra Cranial Access Kit Recalled for Sterile Packaging Defect
Integra LifeSciences is recalling 27 units of its Cranial Access Kit due to defective sterile packaging that may compromise product sterility. The kits were distributed worldwide.
Product
Ref No: HITHSP04 / Integra Cranial Access Kit. For access to the subarachnoid space or the lateral ventricles of the brain.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1209-2024·2024-03-06
Colonoscope Recall: Missing Protective Adhesive May Cause Device Failure
Olympus Corporation is recalling 18 colonoscopes with missing adhesive that protects against physical stress. The missing protective adhesive could allow device failure under vibration, temperature fluctuation, or shock.
Product
Colonoscope, Model Number PCF-H180AL.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0934-2024·2024-03-06
Frozen Pizza Recalled for Undeclared Milk Allergen in Plant-Based Product
Oggi Plant-Based Americana frozen pizza contains undeclared milk, posing a risk to consumers with milk allergies. The recall affects 5,040 units distributed in California, Illinois, and Washington.
Product
Oggi Pizza Plant Based Americana Beyond Meat Crumbles on Cauliflower Crust, gluten-free frozen pizza - cook before serving, net wt. 13.76oz (390g). One pizza wrapped in plastic film in a cardboard box. Retail box UPC 6 28451 68487 9. There are 12 pizza per case, and each case…
Category
Food
Distribution
3 states