State
73,576 recalls have nationwide distribution and so reach California. 13,263 additional recalls listed California specifically in their distribution scope.
Of the 13,263 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 3,368 (25%) are Severe.
Which agencies issued them
These figures cover only the 13,263 recalls whose distribution notice names California specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Amneal Pharmaceuticals is recalling 5,694 Exenatide Injection pens because the delivery system may be defective, potentially leaving the pen empty of medication.
Shantou Qiwei Industrial Co., Ltd is voluntarily recalling 2,970 units of MENOW Sunscreen Pressed Powder SPF35 PA+++ in California due to cGMP deviations.
Medline Industries is recalling 4,013 neurological surgery kits due to potential endotoxin variability that may cause adverse health reactions.
Cardinal Health 200, LLC is recalling Presource Convenience Kits because applicator packaging may have open or incomplete seals, posing a risk of infection.
Starcraft RV is recalling 2022-2024 Super Lite Maxx travel trailers because fasteners may fail, causing the fresh water tank to detach and create a road hazard.
Philips is recalling 387 Achieva 1.5T MRI systems worldwide because a software issue may terminate examinations if manual scan adjustments exceed system memory.
Ventec Life Systems is recalling 25 HomeFill Oxygen Systems because the cylinders lack required medical gas labeling.
Baxter Healthcare is recalling six PRO+ 40-inch MRS Surface mattresses due to errors in the Unique Device Identification (UDI) label text.
Criticare Technologies is recalling 1,007 nGenuity Patient Monitors because a setup error renders the CO2 monitoring function inoperable, potentially delaying procedures.
Baxter Healthcare is recalling two VOLARA systems because contamination in test equipment may have affected flow rate accuracy. Affected devices were returned and confirmed to meet specifications.
DeRoyal Industries is recalling Myocardial Probes that contain an 18mm needle instead of the specified 15mm needle.
Philips is recalling 611 MR 5300 MRI scanners due to a software issue that can terminate examinations during image reconstruction if system memory is exceeded.
Philips is recalling Ingenia 3.0T and 3.0T CX MRI systems because a software issue can terminate examinations during image reconstruction if scan parameters exceed available system memory.
Fresenius Medical Care is recalling CombiSet Hemodialysis Blood Tubing Sets to ensure treatment preparation and handling steps are performed as instructed.
Philips is recalling 91 MRI systems due to a software issue that can terminate examinations during image reconstruction if specific scan parameters are manually adjusted.
Philips is recalling 922 Ingenia Ambition MRI systems due to a software issue that can terminate examinations if system memory is exceeded.
CooperVision is recalling specific lots of Pearle Vision 1 Day contact lenses because a small number of lenses have the incorrect power.
Ventec Life Systems is recalling two HomeFill Oxygen Systems because the cylinders lack required medical gas labeling.
Philips is recalling 37 MR 7700 MRI systems due to a software issue that can terminate examinations during image reconstruction.
Philips is recalling 210 Achieva 3.0T MRI scanners because a software issue can terminate examinations if system memory is exceeded during image reconstruction.
Baxter Healthcare is recalling 169 PRO+ MRS Mattresses because UDI label errors may lead to incorrect product identification or use with incompatible bed frames.
Philips is recalling 82 Intera 1.5T MRI systems worldwide because a software issue can terminate examinations during image reconstruction if specific scan parameters are manually adjusted.
Philips is recalling 2,038 Ingenia 1.5T MRI systems worldwide due to a software issue that can terminate examinations during image reconstruction if specific scan parameters are manually adjusted.
Baxter Healthcare is recalling 824 PRO+ 36-inch MRS Surface mattresses due to errors in the Unique Device Identification (UDI) label. The discrepancies may lead to incorrect product identification or use with incompatible bed frames.
AVID Medical is recalling 192 Halyard IV Start Kits because the included BD ChloraPrep applicators may have open or incomplete packaging seals.