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.
GE Medical Systems is recalling Carescape Central Station units that may not resume patient monitoring for three minutes after a system restart.
Pi-Cardia is recalling 46 ShortCut transfemoral catheters because the positioning arm may detach due to a weld issue.
Bard Access Systems is recalling 22,980 DuoGlide and Niagara short-term dialysis catheters nationwide as a downstream action to a Class I recall.
Howmedica Osteonics Corp. is recalling OMNIFIT Series I acetabular inserts because aged polyethylene material may cause excessive wear and device failure.
BD Switzerland is recalling BD Alaris Pump Infusion Sets due to discrepancies in performance data that may lead to inappropriate pump performance.
Howmedica is recalling specific Scorpio patella implants because aged polyethylene material may cause excessive wear, leading to device failure and potential revision surgery.
Medline Industries is recalling 447 convenience kits nationwide due to potential fungal contamination that could cause serious health consequences.
Abiomed is recalling Impella Optical Controllers because a purge flag component may fail, causing recognition issues. The recall covers 4,100 units distributed in the US and internationally.
Howmedica is recalling 12,156 orthopaedic implant components made with aged polyethylene material. The aging may cause excessive wear, leading to device failure and potential need for revision surgery.
Howmedica Osteonics Corp. is recalling Trident polyethylene knee inserts because aged raw material may cause excessive wear and device failure.
Medline is recalling 10,407 convenience kits containing sterile applicators that may be contaminated with Aspergillus penicillioides, posing a risk of serious infection.
Foods Alive Inc. is recalling 1,691 pouches of organic moringa leaf powder due to potential Salmonella contamination. The product was sold nationwide in the US and UAE.
AVID Medical is recalling Halyard IV Start Kits because they contain applicators contaminated with Aspergillus penicillioides.
Nova Biomedical is recalling StatStrip Glucose meters due to a software defect that may assign patient test results to the wrong medical record.
Abiomed is recalling 1,422 Impella Optical Controllers because a purge flag component may fail, causing purge cassette recognition issues.
Bard Access Systems is recalling Power-Trialysis dialysis catheters as a downstream action to a Class I recall.
Forest River is recalling 2025-2026 Cedar Creek fifth wheel trailers because a sleeper sofa may block the bunkroom door, potentially delaying emergency exits.
Medline Industries is recalling 341 anesthesia pain kits due to open sterile seals that may compromise sterility and lead to patient infection.
Howmedica is recalling specific orthopaedic implant components made with aged UHMWPE material that may oxidize, potentially leading to increased wear and device failure.
ICU Medical is recalling Plum administration sets because drip chambers may contain black specks or discolored PVC material. The presence of particulate matter in the fluid path has not been ruled out.
Datex-Ohmeda is recalling 410 Et Control software units for anesthesia gas machines that may interrupt anesthetic delivery, requiring clinician intervention to prevent decreased patient effect.
Maquet is recalling Percutaneous Insertion Kits because the packaging may not consistently maintain sterile barrier integrity, posing a risk of infection.
Medline Industries is recalling 459 units of Minor Pack convenience kits because open sterile seals may compromise sterility and lead to patient infection.
Medline is recalling 135 Open Heart A Pack kits in California due to a potential sterile barrier breach in the RCSP cannulae, posing a risk of infection.
Happiest Baby, Inc is recalling 1,055 units of SNOO Sleep Sacks because Extra Small and Extra Large sizes have not been reviewed for safety and effectiveness by the FDA.