The Recall Desk

State

California product recalls

73,104 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.

These figures cover only the 13,251 recalls whose distribution notice names California specifically. The 73,104 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

10951–10975 of 86355

  • 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
  • HighFDA (Devices)·Z-2979-2024·2024-09-11

    Power Express PE Centrifuge adhesive joint failure may cause component detachment

    The adhesive joint in this medical device component can fail, causing the metal part to detach. This may damage the centrifuge, destroy patient samples, and potentially expose lab staff to biohazardous material.

    Product
    PE Centrifuge, REF: B36365, a component of the Power Express
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V667000·2024-09-11

    Ember Recalls 2023-2024 Travel Trailers Due to Incorrect Cargo Capacity Labels

    Ember is recalling 2023-2024 E-Series, Overland Series, and Touring Edition travel trailers because certification labels list incorrect cargo carrying capacity, which can allow the trailer to become overloaded.

    Product
    EMBER — EMBER E-SERIES, OVERLAND SERIES, TOURING EDITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1769-2024·2024-09-11

    Reser's Banana Pudding Kit Recalled Due to Temperature Abuse

    Reser's Fine Foods recalls 6 cases of Item 71117.03034 Banana Pudding Kit due to temperature abuse from a malfunctioning refrigeration unit. Affected products were distributed to CA, IL, MN, ND, and SD.

    Product
    Item 71117.03034, Reser's Kit HF Pudding Banana, refrigerated product, net wt. 4.81lb. There are 2 packs per case.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-2946-2024·2024-09-11

    W L Gore Recalls Heparin Viabahn VBX Endoprosthesis Due to Packaging Defects

    W L Gore & Associates is recalling specific lots of Heparin, Gore Viabahn VBX Balloon Expandable Endoprosthesis because packaging defects may compromise sterility and heparin activity.

    Product
    Heparin, Gore Viabahn VBX, Balloon Expandable Endoprosthesis, for the following Reference numbers: United States: BXB055902C, BXB063902C, BXB065902C, BXB067902C, BXB073902C, BXB075902C, BXB077902C, BXB083902C, BXB085902C, BXB087902C, BXB093902C, BXB095902C, BXB097902C…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2971-2024·2024-09-11

    Impella 5.5 Cardiac Pump Recalled for Undocumented Device Interaction

    Abiomed recalled 413 units of Impella 5.5 with SmartAssist S2 pumps worldwide due to a potential undocumented interaction with Shockwave coronary catheters during cardiac procedures. The company will update product labeling to disclose this interaction.

    Product
    Impella 5.5 with SmartAssist S2 Set, EU; Product Code: 1000482;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1778-2024·2024-09-11

    Reser's Sweet Corn with Butter recalled due to temperature abuse

    Reser's recalls 104 cases of sweet corn with butter due to shipment temperature abuse that may cause spoilage. Use By date Sept. 9, 2024; distributed in CA, IL, MN, ND, and SD.

    Product
    Item 71117.56013, Reser's Sweet Corn with Butter, refrigerated product, net wt. 4lb. There are 4 packs per case.
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-2957-2024·2024-09-11

    Abiomed updates Impella CP labeling for Shockwave coronary catheter interaction

    Abiomed is recalling the Impella CP Pump 371 Set due to a potential device interaction with the Shockwave Coronary IVL Catheter. The manufacturer is updating labeling to address this interaction. No illnesses or injuries have been reported.

    Product
    Impella CP Pump 371 Set, Clinical Trial; Product Code: 0048-0040;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2961-2024·2024-09-11

    Impella 5.5 with SmartAssist Set: Potential Device Interaction During Coronary Interventions

    Abiomed is updating labeling for Impella 5.5 with SmartAssist Set due to a potential device interaction with Shockwave Coronary IVL Catheter during coronary interventions. The product labeling currently lacks information about this potential interaction.

    Product
    Impella 5.5 with SmartAssist Set, EU; Product Code: 0550-0002;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2954-2024·2024-09-11

    Impella CP Smart Assist Set: Device interaction safety labeling update

    Abiomed is updating labeling for the Impella CP Smart Assist Set to address a potential device interaction with the Shockwave Coronary IVL Catheter during coronary procedures. No illnesses or injuries have been reported.

    Product
    Impella CP Smart Assist Set, EU; Product Code: 0048-0014;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1768-2024·2024-09-11

    Reser's Asiago Creamed Spinach recalled due to potential spoilage

    Reser's Fine Foods recalls Asiago Creamed Spinach due to potential spoilage from temperature abuse during transport. The affected product has a use-by date of August 31, 2024.

    Product
    Item 71117.02126, Reser's American Classics Asiago Creamed Spinach, refrigerated product, net wt. 12oz. There are 6 packs per case.
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-1765-2024·2024-09-11

    Reser's Essential Everyday Potato Salad recalled for spoilage risk from temperature abuse

    Reser's Essential Everyday Original Potato Salad recalled due to potential spoilage from temperature abuse affecting refrigerated units. Affected cases distributed in CA, IL, MN, ND, and SD.

    Product
    Item 41303.82013, Reser's Essential Everyday Original Potato Salad, refrigerated product, net wt. 16oz. There are 6 packs per case.
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-2953-2024·2024-09-11

    Philips Azurion 7M20 Fluoroscopic X-Ray System FlexArm Movement Recall

    Philips Azurion 7M20 interventional fluoroscopic X-ray systems with FlexArm ceiling-mounted stands may experience inconsistent or unavailable longitudinal movement due to bearing grease leakage affecting device mobility. Approximately 927 systems worldwide are affected.

    Product
    Philips Azurion 7M20 systems with FlexArm ceiling-mounted system, Interventional Fluoroscopic X-Ray System, Model Numbers 722079 and 722224
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1772-2024·2024-09-11

    Reser's Egg Salad Recalled Due to Temperature Abuse During Shipping

    Reser's American Classics Egg Salad has been recalled due to potential spoilage caused by temperature abuse from a malfunctioning refrigeration unit. The affected product was distributed in five states.

    Product
    Item 71117.11356, Reser's American Classics Egg Salad, refrigerated product, net wt. 12oz. There are 6 packs per case.
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-2969-2024·2024-09-11

    Impella CP Smart Assist Set: Potential Device Interaction with Coronary Catheter

    Abiomed is updating labeling for the Impella CP Smart Assist Set to address a potential device interaction with the Shockwave Coronary IVL Catheter during coronary procedures.

    Product
    Impella CP Smart Assist Set; Product Code: 1000402;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2960-2024·2024-09-11

    Impella CP Cardiac Assist Pump Lacks Shockwave Catheter Interaction Warning

    Abiomed is updating labeling for Impella CP Smart Assist pumps to address a potential interaction with Shockwave Coronary IVL Catheters during coronary interventions. The interaction was previously undocumented in device labeling.

    Product
    Impella CP Smart Assist Set APAC; Product Code: 0048-0047;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2963-2024·2024-09-11

    Abiomed Impella 5.5 Recall for Potential Shockwave Catheter Interaction

    Abiomed is recalling 2,916 Impella 5.5 units to update labeling regarding a potential interaction with Shockwave Coronary IVL Catheters during coronary interventions.

    Product
    Impella 5.5 with SmartAssist Set, US; Product Code: 0550-0008;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2959-2024·2024-09-11

    Abiomed Impella Pump Recall for Potential Shockwave Catheter Interaction

    Abiomed is recalling 43,636 Impella Pumps to update instructions for use regarding a potential interaction with Shockwave Coronary IVL Catheters.

    Product
    Pump 371 14F LT CMR Set; Product Code: 0048-0045;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1770-2024·2024-09-11

    Reser's Macaroni & Cheese Recalled for Temperature Abuse During Shipment

    Reser's American Classics Macaroni & Cheese (12 oz) is recalled because a malfunctioning refrigeration unit caused temperature abuse during shipment, which may cause spoilage.

    Product
    Item 71117.02123, Reser's American Classics Macaroni & Cheese, refrigerated product, net wt. 12oz. There are 6 packs per case.
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-1773-2024·2024-09-11

    Baked Scalloped Potatoes Recalled Due to Temperature Abuse During Distribution

    Reser's Fine Foods recalls Baked Scalloped Potatoes due to potential spoilage from temperature abuse during shipment. Affected products have Use By dates of September 11–13, 2024.

    Product
    Item 71117.14378, Baked Scalloped Potatoes Special Request, refrigerated product, net wt. 2.5lb. There are 8 packs per case.
    Category
    Food
    Distribution
    5 states