State

California product recalls

72,940 recalls have nationwide distribution and so reach California. 13,245 additional recalls listed California specifically in their distribution scope.

What the numbers show

Total: 13,245
Critical: 1,605
Severe: 2,843
Most recent: 2026-09-09

Of the 13,245 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 2,843 (21%) are Severe.

Which agencies issued them

These figures cover only the 13,245 recalls whose distribution notice names California specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4526–4550 of 86185

HighFDA (Devices)·Z-0720-2026·2025-12-03
Anesthesia vaporizers recalled over the potential for anesthesia leakage
Mindray is recalling 148 Sevoflurane V90 Electronic Vaporizers used with the A9 Anesthesia System over the potential for anesthesia leakage.
Product
Sevoflurane (SEVO) V90 Electronic Vaporizer with the A9 Anesthesia System. Labeled as the following: 1. Sev E_Vap. (Safety Filling adapter), Part Number: 115-066756-00. 2. Exchange Sev E_Vap. (Safety Filling adapter), Part Number: E115-066756-00. Product Description: Th
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0723-2026·2025-12-03
Imaging software recalled over a bug that can lose clinical information
Intelerad Medical Systems is recalling 19 IntelePACS InteleConnect and TechPortal installations because a bug can cause data loss in the Relevant Clinical Info field.
Product
IntelePACS - InteleConnect / TechPortal
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0583-2026·2025-12-03
Skin cancer aid recalled because it may not meet specifications
DermaSensor is recalling nine affected units of its software-aided diagnostic device because it may not meet specifications, risking incorrect results or a delayed referral.
Product
DermaSensor. Model/Catalog Number: 10101. Software Version: 3.0.2. Software-aided adjunctive diagnostic device for use by physicians on lesions suspicious for skin cancer
Category
Medical Device
Distribution
8 states
HighFDA (Food)·H-0207-2026·2025-12-03
Ice cream bars recalled over undeclared wheat and soy allergens
Jeni's Splendid Ice Creams is recalling 3,767 cases of Passion Fruit Dreamsicle Ice Cream Bars over undeclared wheat and soy.
Product
Jeni's Passion Fruit Dreamsicle Ice Cream Bars, 3 FL OZ (89 ML)/9 FL OZ (266 ML), packaged 3 bars per retail carton with Item UPC: 850060644122, packed 8 retail cartons per case with Case UPC: 10850060644129
Category
Food
Distribution
10 states
HighFDA (Devices)·Z-0589-2026·2025-12-03
Vena cava filters recalled over resistance when advancing the dilator
Argon Medical Devices is recalling 1,821 Option ELITE Vena Cava Filter Systems after complaints of increased resistance when advancing the dilator within the introducer sheath.
Product
Option"ELITE Vena Cava Filter System REF 352506070E UDI-DI code: 00886333217151 The Option"ELITE Filter is indicated for the prevention of recurrent pulmonary embolism (PE) via percutaneous placement in the inferior vena cava (IVC) in the following conditions: " Pulmonary t
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0598-2026·2025-12-03
Anesthesia set 490469 recalled over backflow and priming occlusion
B. Braun Medical is recalling 104,784 units anesthesia iv sets over the potential for medication backflow from secondary piggyback containers and an inability to prime.
Product
Brand Name: Galaxy System Product Name: Galaxy System Model/Catalog Number: GAL-001 Product Description: The Galaxy SystemTM and its accessories are intended to provide bronchoscopic visualization of and access to patient airways for diagnostic and therapeutic procedure.
Category
Medical Device
Distribution
20 states
HighFDA (Devices)·Z-0722-2026·2025-12-03
Hot and cold wraps recalled over microwave instructions causing burns
DJO is recalling 1,594 Cold Form Wraps because the instructions tell users to microwave the wrap for three minutes, which may cause leaks or second degree burns.
Product
Cold Form Wrap: Back, REF: DP163CT03-BLK-L,XL, and Shoulder, REF: DP163CT02
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0578-2026·2025-12-03
IV set 490487 recalled over piggyback backflow and occlusion risk
B. Braun Medical is recalling 23,160 units iv administration sets over the potential for medication backflow from secondary piggyback containers and an inability to prime.
Product
FoundationOne Liquid CDx (F1LCDx), TECH-0009 version 6.0
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0192-2026·2025-12-03
Tinted mineral sunscreen recalled over manufacturing practice deviations
CA Botana International is recalling 2,090 tubes of Sugared+Bronzed Tinted Mineral Sunscreen SPF 50 for CGMP deviations.
Product
Sugared+Bronzed Tinted Mineral Sunscreen SPF 50, Zinc Oxide 21%, Net WT 3.3 OZ (93 G) per tube, Dist. By: Sugared+Bronzed, 929 Montana Ave, Santa Monica, CA 90403. NDC: 35192-055-18, UPC 8 50047 92223 6
Category
Drug
Distribution
5 states
ModerateFDA (Drugs)·D-0185-2026·2025-12-03
Tea tree balm recalled over current good manufacturing practice deviations
CA Botana International is recalling 555 tubes of Doctor D. Schwab Controlling Balm with Tea Tree Oil for CGMP deviations.
Product
Doctor D. Schwab Controlling Balm with Tea Tree Oil, Salicyclic Acid 0.8%, 1 FL OZ/ 30 ML per tube, Doctor D. Schwab, A division of CA BOTANA, San Diego, CA 92123. NDC: 35192-016-05
Category
Drug
Distribution
5 states
ModerateFDA (Devices)·Z-0581-2026·2025-12-03
Vitrectomy probe packs recalled with no reason stated in the record
Alcon Research is recalling 28,323 Constellation UltraVit 10K and HyperVit 20K vitrectomy probe packs; the enforcement record does not state a reason.
Product
CONSTELLATION ULTRAVIT 10K and CONSTELLATION HYPERVIT 20K, Description/REF: 25+ TOTALPLUS CP PAK 20K CPM BWV .9 IU/ 8065000093; 25+ TOTALPLUS CP PAK 20K CPM BV .9 IU/ 8065000095; 27+ TOTALPLUS CP PAK 20K CPM BV .9 IU/ 8065000096; 23GA BEVEL ULTRAVIT 10,000 CPM/ 8065752413; 25+ B
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0188-2026·2025-12-03
Menthol arnica gel recalled over current good manufacturing practice deviations
CA Botana International is recalling 810 tubes of Doctor D. Schwab Clinical Weh Weh Natural Pain Relief Gel with Menthol and Arnica for CGMP deviations.
Product
Doctor D. Schwab Clinical Weh Weh Natural Pain Relief Gel with Menthol and Arnica, Menthol 5%, 4.2 oz./120 g per tube, Doctor D. Schwab, A division of CA BOTANA, San Diego, CA 92121. NDC: 35192-020-02
Category
Drug
Distribution
5 states
ModerateFDA (Devices)·Z-0724-2026·2025-12-03
Tuberculosis test cartridges recalled after failing expected stability criteria
Cepheid is recalling 9,880 Xpert MTB/RIF cartridges from one lot because product testing did not meet expected stability criteria.
Product
Xpert MTB/RIF. Model Number: GXMTB/RIF-US-10.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0183-2026·2025-12-03
Schwab mineral sunscreen recalled over manufacturing practice deviations at Botana
CA Botana International is recalling 1,167 tubes of Doctor D. Schwab Mineral Sunscreen SPF 50 for CGMP deviations.
Product
Doctor. D. Schwab Mineral Sunscreen SPF 50, Zinc Oxide 21%, 4 oz./ 113.4 g per tube, Manufactured by CA Botana, San Diego, CA 92123. NDC: 35192-042-02
Category
Drug
Distribution
5 states
ModerateFDA (Devices)·Z-0585-2026·2025-12-03
Culture media recalled over contamination that may darken the broth
Remel is recalling cation-adjusted Mueller Hinton broth and Brucella broth because the products may contain contamination, which may result in a darker or brown media color.
Product
1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0196-2026·2025-12-03
Menthol pain relief gel recalled over manufacturing practice deviations
CA Botana International is recalling 4,890 bottles of Dr. Bump Natural Pain Relief Gel with Menthol 5% for CGMP deviations.
Product
Dr. Bump Natural Pain Relief Gel, Menthol 5%, NET WT 4 FL OZ/118 ML per bottle, Distr. by 1Beauty US LLC, Palm Desert, CA 92211. NDC: 35192-052-18, UPC 8 18204 02513 8
Category
Drug
Distribution
5 states
ModerateFDA (Devices)·Z-0577-2026·2025-12-03
Cancer test reports recalled for omitting the companion diagnostic claims page
Foundation Medicine is recalling 59 FoundationOne CDx reports that were sent to customers without the companion diagnostic Claims Page.
Product
FoundationOne CDx (F1CDx), RAL-0003 version 31.0
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0195-2026·2025-12-03
CLEARSTEM sunscreen recalled over current good manufacturing practice deviations
CA Botana International is recalling 4,890 bottles of CLEARSTEM You Are Sunshine SPF 50 for CGMP deviations.
Product
CLEARSTEM YOU ARE SUNSHINE SPF 50, Zinc Oxide 21%, 2.1 oz/61g per bottle, Distributed by: CLEARSTEM Skincare, clearstemskincare.com. NDC: 35192-046-17
Category
Drug
Distribution
5 states
ModerateFDA (Drugs)·D-0190-2026·2025-12-03
Gabriel mineral sunscreen recalled over manufacturing practice deviations
CA Botana International is recalling 1,617 tubes of Gabriel Mineral Sunscreen SPF 50 for CGMP deviations.
Product
Gabriel Mineral Sunscreen SPF 50, Zinc Oxide 21%, 2.1 oz, Net 61 g per tube, Dist. By: Gabriel Cosmetics, Inc., Redmond, WA USA 98052, NDC: 35192-044-01, UPC 7 07060 9592 1
Category
Drug
Distribution
5 states
ModerateFDA (Drugs)·D-0191-2026·2025-12-03
Daily moisturizer recalled over current good manufacturing practice deviations
CA Botana International is recalling 1,492 tubes of Karina Daily Moisturizer SPF 25 for CGMP deviations.
Product
Karina Daily Moisturizer SPF 25, Octinoxate 7.5% and Zinc Oxide 7.0%, Net WT. 5 oz/ 141.7 g per tube, Dist. By: Beauty4Pros LLC, Palm Desert, CA 92211. NDC: 35192-033-16, UPC 8 18204 02572 5
Category
Drug
Distribution
5 states
ModerateFDA (Drugs)·D-0194-2026·2025-12-03
Elixir tinted sunscreen recalled over manufacturing practice deviations
CA Botana International is recalling Elixir by Coco March Tinted Mineral Sunscreen SPF 50 for CGMP deviations.
Product
Elixir by Coco March Tinted Mineral Sunscreen SPF 50, Zinc Oxide 21%, 2.1 oz (62g) per bottle, Distributed by: VitaTienda Co U.S.A., San Juan, PR 00646. NDC: 35192-050-17, UPC 6 7229 99913 8
Category
Drug
Distribution
5 states
ModerateFDA (Drugs)·D-0186-2026·2025-12-03
Benzoyl peroxide cream recalled over current good manufacturing practice deviations
CA Botana International is recalling 470 tubes of Doctor D. Schwab Controlling Cream with Benzoyl Peroxide 2.7% for CGMP deviations.
Product
Doctor D. Schwab Controlling Cream, Benzoyl Peroxide 2.7%, 1 FL OZ/ 30 ML per tube, Doctor D. Schwab, A division of CA BOTANA, San Diego, CA 92123. NDC: 35192-017-05
Category
Drug
Distribution
5 states
ModerateFDA (Drugs)·D-0187-2026·2025-12-03
Mineral sunscreen recalled over current good manufacturing practice deviations
CA Botana International is recalling 874 tubes of Sea Enzyme Ultra Umbrella Sunscreen SPF 30 for CGMP deviations.
Product
Sea Enzyme Ultra Umbrella Sunscreen SPF 30, Titanium Dioxide 4%, Octinoxate 4%, 4 oz./113.4 g per tube, Manufactured by CA BOTANA, San Diego, CA 92121. NDC: 35192-011-02
Category
Drug
Distribution
5 states
ModerateFDA (Drugs)·D-0193-2026·2025-12-03
Mineral sunscreen recalled over current good manufacturing practice deviations
CA Botana International is recalling 3,295 bottles of Elixir by Coco March Mineral Sunscreen SPF 50 for CGMP deviations.
Product
Elixir by Coco March Mineral Sunscreen SPF 50, Zinc Oxide 21%, 2.1 oz (62g) per bottle, Distributed by: VitaTienda Co U.S.A., San Juan, PR 00646. NDC: 35192-048-17, UPC 8 10145 82007 0
Category
Drug
Distribution
5 states
ModerateFDA (Devices)·Z-0719-2026·2025-12-03
Interventional imaging systems recalled over ceiling rail movement that may fail
Philips is recalling 172 Azurion 7M20 systems with FlexArm because motorized longitudinal movement of the stand may be inconsistent and eventually become unavailable.
Product
Philips Azurion 7M20 systems with FlexArm ceiling-mounted system. Model Number: 722234;
Category
Medical Device
Distribution
28 states