State

California product recalls

73,100 recalls have nationwide distribution and so reach California. 13,251 additional recalls listed California specifically in their distribution scope.

What the numbers show

Total: 13,251
Critical: 1,605
Severe: 2,846
Most recent: 2026-09-25

Of the 13,251 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 2,846 (21%) are Severe.

Which agencies issued them

These figures cover only the 13,251 recalls whose distribution notice names California specifically. The 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

10926–10950 of 86351

HighFDA (Devices)·Z-2949-2024·2024-09-11
Sevoflurane Vaporizer for A9 Anesthesia System Recalled for Output Malfunction
Mindray recalled 2 Sevoflurane E_Vap vaporizers used in A9 Anesthesia Systems due to a component defect causing excessive anesthetic output. The defect risks patient anesthetic overdose with potential neurological effects including post-operative vertigo and drowsiness.
Product
Sevoflurane E_Vap.(Quik-Fil):used with the A9 Anesthesia System-Used to provide the vapor of an anesthetic agent with controllable concentration to an A9 anesthesia system. Part Number 115-066755-00
Category
Medical Device
Distribution
8 states
HighFDA (Drugs)·D-0655-2024·2024-09-11
Tirzepatide Injectable Vials Recalled for Sterility Assurance
ProRx LLC is recalling Tirzepatide 20 mg/2mL injectable vials nationwide due to lack of assurance of sterility. Patients who received vials from lot ProRx051424 should contact their healthcare provider.
Product
TIRZEPATIDE 20 mg/2mL (10/mg/mL), Rx Only, 2mL Multiple Dose Vial, Mfd by: ProRx Exton, PA, 19341, NDC 84139-210-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0652-2024·2024-09-11
Compounded Semaglutide Injection Vials Recalled for Sterility Concerns
ProRx LLC is recalling approximately 8,396 vials of compounded semaglutide due to lack of assurance of sterility. The medication was distributed nationwide.
Product
SEMAGLUTIDE 5mg/2mL (2.5mg/mL), Rx Only 2 mL Multiple Dose Vial, Rx Only, Compounded Drug, Mfd by: ProRX Exton, PA19341, NDC 84139-225-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0654-2024·2024-09-11
ProRx Compounded Semaglutide/Cyanocobalamin Injection Recalled Due to Sterility Assurance Issues
ProRx LLC is recalling 500 vials of compounded Semaglutide/Cyanocobalamin Injection (Lot #ProRx031924-1) distributed nationwide in the United States due to lack of sterility assurance. The beyond-use date is 09/18/2024.
Product
Semaglutide / Cyanocobalamin Injection: 2.5/0.5 mg/mL, 2 mL Multiple Dose Vial, Compounded Rx Product, ProRX 267-565-7008, NDC 84139-225-02
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·24V664000·2024-09-11
Airstream Recalls 2025 Classic Travel Trailers Due to Fire Risk
Airstream is recalling 2025 Classic travel trailers because a power hub may overheat, increasing the risk of a fire.
Product
AIRSTREAM — AIRSTREAM CLASSIC
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-1766-2024·2024-09-11
Reser's American Classics Scalloped Potatoes Recalled Due to Temperature Abuse
Reser's Fine Foods is recalling Reser's American Classics Scalloped Potatoes because a refrigeration unit malfunction caused temperature abuse during shipment, potentially leading to spoilage. Consumers should not consume this product.
Product
Item 71117.02008, Reser's American Classics Scalloped Potatoes, refrigerated product, net wt. 12oz. There are 6 packs per case.
Category
Food
Distribution
5 states
HighFDA (Devices)·Z-2966-2024·2024-09-11
Impella 5.5 Pump Labeling Updated Due to Device Interaction
Abiomed updated Impella 5.5 cardiac pump labeling to document a potential interaction with Shockwave Coronary IVL Catheter during coronary procedures. No injuries have been reported.
Product
Impella 5.5 SmartAssist Set, JP; Product Code: 1000211;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0656-2024·2024-09-11
Tirzepatide Injectable Drug Recalled for Sterility Assurance Defect
ProRx LLC is recalling 1,732 vials of Tirzepatide 60 mg/3mL nationwide due to lack of assurance of sterility. Affected lots have beyond-use dates of 11/21/2024 and 12/09/2024.
Product
TIRZEPATIDE 60 mg/3mL (20/mg/mL), Rx Only, 3mL Multiple Dose Vial, Mfd by: ProRx Exton, PA, 19341, NDC 84139-210-02
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2950-2024·2024-09-11
Anesthesia Vaporizer Adapter May Deliver Excessive Anesthetic Concentration
Sevoflurane vaporizer adapters used with Mindray A9 anesthesia systems may deliver higher-than-set anesthetic concentrations due to incomplete sealing. Patients could inhale excessive anesthetic, potentially causing drowsiness, vertigo, or in severe cases, neurological effects.
Product
Sevoflurane E_Vap.(Safety Filling adapter) used with the A9 Anesthesia System-Used to provide the vapor of an anesthetic agent with controllable concentration to an A9 anesthesia system. Part Number: 115-066756-00
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-2978-2024·2024-09-11
Medical Device Sample Holder Recalled for Adhesive Joint Failure
Beckman Coulter Power Express sample holders can fail at the adhesive joint between plastic socket and metal component. This may cause the metal part to detach inside the centrifuge, potentially damaging equipment and exposing lab staff to biohazardous material.
Product
Power Express, REF B90918
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2958-2024·2024-09-11
Impella CP Smart Assist Set device interaction with coronary catheters
The FDA is recalling Impella CP Smart Assist Sets due to a potential device interaction with Shockwave Coronary IVL Catheters used during coronary interventions. Abiomed will update device labeling to inform users about this interaction.
Product
Impella CP Smart Assist Set, Canada; Product Code: 0048-0044;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2970-2024·2024-09-11
Impella 5.5 SmartAssist S2 Labeling Updated for Shockwave Catheter Interaction
Abiomed is updating labeling for the Impella 5.5 SmartAssist S2 cardiac assist device to address a potential interaction with Shockwave Coronary IVL Catheters during coronary interventions.
Product
Impella 5.5 SmartAssist S2 Set, JP; Product Code: 1000459;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2951-2024·2024-09-11
Anesthesia System Vaporizer Adapter Recalled for Potential Anesthetic Overdose
Mindray's Isoflurane E_Vap adapter for the A9 Anesthesia System is recalled due to a seal defect that may cause higher-than-intended anesthetic concentration delivery. Twenty-four units were distributed to eight U.S. states and Canada.
Product
Isoflurane E_Vap.(Safety Filling adapter): used with the A9 Anesthesia System-Used to provide the vapor of an anesthetic agent with controllable concentration to an A9 anesthesia system. Part Number: Part Number 115-066758-00
Category
Medical Device
Distribution
8 states
HighFDA (Food)·F-1775-2024·2024-09-11
Reser's Homestyle Gravy Recalled Due to Temperature Abuse
Reser's Fine Foods recalls Item 71117.14459 Gravy Homestyle due to temperature abuse during shipping. The product may become spoiled and pose food safety risks.
Product
Item 71117.14459, Gravy Homestyle, refrigerated product, net wt. 4lb. There are 3 packs per case.
Category
Food
Distribution
5 states
HighFDA (Devices)·Z-2948-2024·2024-09-11
BD Pyxis QFill Medication Cabinet Software Bug Causes Incorrect Restock Labels
The BD Pyxis QFill Replenishment Station medication cabinet has a software issue that may print incorrect bin information on restock labels for medications stored in non-CUBIE locations.
Product
BKIT BD Pyxis QFill Replenishment Station, REF: 155197-01, medication cabinet system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2955-2024·2024-09-11
Impella CP Smart Assist Set Lacks Labeling for Potential Device Interaction
Abiomed is updating labeling for the Impella CP Smart Assist Set to warn about a potential interaction with the Shockwave Coronary IVL Catheter when used during coronary interventions. The interaction was previously undocumented in the device instructions.
Product
Impella CP Smart Assist Set, JP; Product Code: 0048-0024-JP;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2956-2024·2024-09-11
Impella CP Pump Set Recalled for Potential Device Interaction
Abiomed is recalling the Impella CP Pump Set due to a potential device interaction with the Shockwave Coronary IVL Catheter during coronary interventions. The manufacturer will update device instructions to address this interaction.
Product
Impella CP Pump Set, Japan; Product Code: 0048-0034-JP;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2964-2024·2024-09-11
Pump 381 Pump Set lacks labeling for Shockwave catheter interaction risk
Abiomed's Pump 381 Pump Set labeling lacks information about potential interactions with Shockwave Coronary IVL Catheters during coronary interventions. The manufacturer is updating instructions for use to address this gap.
Product
Pump 381 Pump Set (US); Product Code: 1000080;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1776-2024·2024-09-11
Reser's Raspberry Parfait Desserts Recalled for Potential Spoilage
Reser's Fine Foods recalls 18 cases of Raspberry Parfait Desserts due to temperature abuse during transport that may have caused spoilage. Products with use-by date 12/4/2024 distributed in CA, IL, MN, ND, and SD.
Product
Item 71117.15207, Reser's Raspberry Parfait Desserts, refrigerated product, net wt. 8lb. There are 2 packs per case.
Category
Food
Distribution
5 states
HighFDA (Drugs)·D-0650-2024·2024-09-11
Compounded semaglutide injection recalled due to sterility concerns
ProRx LLC is recalling compounded semaglutide injections due to lack of assurance of sterility. The recall affects 2,490 vials distributed nationwide.
Product
Semaglutide, 2 mL (2.5mg/mL), Compounded RX Product, Multidose SC inj, glass vial, ProRx, 267-565-7008, NDC 84139-225-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2965-2024·2024-09-11
Impella 5.5 Device Recalled for Missing Labeling on Catheter Interaction
Abiomed is updating labeling for Impella 5.5 cardiac support pumps to include information about a potential device interaction with Shockwave Coronary IVL Catheters during coronary interventions.
Product
Impella 5.5 with SmartAssist S2 Set, US; Product Code: 1000100;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1771-2024·2024-09-11
Reser's Smokehouse Potato Salad Recalled Due to Spoilage Risk
Reser's Fine Foods is recalling 7 cases of Smokehouse Potato Salad due to potential spoilage from temperature abuse during shipping. No illnesses have been reported.
Product
Item 71117.10923, Reser's Smokehouse Potato Salad, refrigerated product, net wt. 5lbs. There are 2 packs per case.
Category
Food
Distribution
5 states
HighFDA (Devices)·Z-2980-2024·2024-09-11
Beckman Power Express Centrifuge Sample Holder May Detach During Operation
An adhesive joint failure in the PE Centrifuge Temperature Controlled component can cause the metal part to detach inside the centrifuge, risking sample destruction and potential exposure of laboratory technicians to biohazardous material.
Product
PE Centrifuge Temperature Controlled, REF: B36366, a component of the Power Express.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2945-2024·2024-09-11
Heparin Gore Viabahn VBX Endoprosthesis Recalled for Packaging Defects
W L Gore & Associates is recalling Heparin Gore Viabahn VBX Balloon Expandable Endoprosthesis devices due to packaging defects that may compromise sterility assurance and heparin activity.
Product
Heparin, Gore Viabahn VBX, Balloon Expandable Endoprosthesis, for the following Reference numbers: United States: BXB051501A BXB051502A BXB051901A BXB051902A BXB052901A BXB052902A BXB053901A BXB053902A BXB055901A BXB055902A BXB057901A BXB057902A BXB061501A BXB061502A…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0651-2024·2024-09-11
Compounded Tirzepatide Injectable Vials Recalled for Sterility Assurance Issues
ProRx LLC is recalling 37 vials of compounded Tirzepatide injectable due to lack of sterility assurance. The 2 mL vials (10 mg/mL and 20 mg/mL) were distributed nationwide.
Product
Tirzepatide 2 mL (10 mg/mL) and 20 mg/mL, 2mL Multidose SC Injection vials, Compounded Rx Product, ProRx 267-565-7008, NDC 84139-210-01
Category
Drug
Distribution
Distributed nationwide