Recalls distributed in California
These notices name California in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
7,403 stored notices name California, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach California too — those are in the archive.
Reported May 13, 2020
R-F Injector Cannula. 18gx10cm-STERILE. REF/UDI: 257-1810/(01)00828788021496; REF/UDI: 257-1810D(01)10818788021493 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Epimed International
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 13, 2020
Benefiber Healthy Shape Prebiotic Fiber Supplement, 500G UPC 886790018872
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Glaxosmithkline Consumer Healthcare Holdings
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 13, 2020
Cortoss Bone Augmentation Material, Catalog Nos. 2101-0005 and 2101-0010
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
FDA (openFDA device enforcement)
Reported May 13, 2020
REF: AH7117 111" 10 Drop Admin Set w/2 Inj Sites, Rotating Luer, Sterile R, For Veterinary Use Only, (01) 1 0887709…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
10 more products in this recall
FDA (openFDA device enforcement)
Reported May 13, 2020
Inpeco FlexLab Centrifuge Module tube loading algorithm, Inpeco SA P/N: FLX-202, with Firmware Versions: CM_1-7-0.H86…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Inpeco S.A.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 13, 2020
da Vinci Xi Surgical System, IS4000 - Product Usage: The da Vinci Xi surgical system (IS4000) is made of three main…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 13, 2020
daVinci XI Sureform 60 reload, 60 mm Green 6- Row, 4.6 mm, REF 48360G-08, UDI: 00886874113844, Rx Only, Sterile EO -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 13, 2020
Visualase Cooled Laser Applicator System Tubing Set kits Product numbers: VCLAS 9735559, 3mm tip/1.65mm catheter VCLAS…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported May 13, 2020
NUVASIVE MAGEC 2 Rod X.X mm XX mm, REF MC2-XXXXS LOT 0000000 AAA - Product Usage: comprised of a sterile single-use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NuVasive Inc.
FDA (openFDA device enforcement)
Reported May 13, 2020
Tibial Tray Nonporous A Size 2; Model # PN 162-1200-A; Material: Ti6Al4V.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho Development Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 13, 2020
3.5mm Aresenal Screw Drill Bit , Ref: 330-35-001, Qty. 70, Rx Only, Non-Sterile, UDI: (01)00812926029696 - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trilliant Surgical, LLC
FDA (openFDA device enforcement)
Reported May 13, 2020
Varian Multileaf Collimator [MLC]; Millenium Multileaf Collimator [52, 80, 120 leaf]; High Definition 120 Multileaf…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Varian Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported May 12, 2020
Ideal Foods Recalls Meat and Poultry Flatbread Pizza Products Produced Without Benefit of Inspection
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ideal Foods
USDA FSIS
Reported May 6, 2020
CORFLO Percutaneous Endoscopic Gastrostomy (PEG)Kit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Avanos Medical, Inc.
FDA (openFDA device enforcement)
Reported May 6, 2020
Autoimmune EIA Anti-Tissue Transglutaminase (tTG) IgA Test; Material Number 425-2260; Lot number 18200A - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Labs
FDA (openFDA device enforcement)
Reported May 6, 2020
CapsoCAM Plus, UDI: 00867770000209
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Capso Vision, Inc.
FDA (openFDA device enforcement)
Reported May 6, 2020
ICU Medical Cogent Hemodynamic Monitoring System, Cogent Item Number 58400-000, UDI: (01)00840619079499
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
FDA (openFDA device enforcement)
Reported May 6, 2020
Nexus Universal with OptiBond Universal, Universal Adhesive Resin Cement, Trial Kit, Ref # 36990 - Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kerr/Pentron, dba Kerr Corporation and Pentron Clinical
FDA (openFDA device enforcement)
Reported May 6, 2020
PreludeSYNC DISTAL Radial Compression Devices, SDRB-REG-LT, SDRB-REG-RT
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported May 6, 2020
5.5 oz cans of Ocean Spray Pink Lite Cranberry Juice Drink
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ocean Spray Cranberries Inc.
FDA (openFDA food enforcement)
Reported May 6, 2020
Phillips Azurion 7 M20, Angiographic X-Ray System Code 722079 Image guidance in diagnostic, interventional and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 6, 2020
ABL800 FLEX model number 393-800 and 393-801, UDI:(01)05700693938004
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
FDA (openFDA device enforcement)
Reported May 6, 2020
Velofix SA cervical cage, REF: TSA161207, TSA161208, TSA161209, TSA161210, TSA161407, TSA161408, TSA161409, TSA161410 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.U&i Corp.
FDA (openFDA device enforcement)
Reported May 6, 2020
ProACT Implantation Instrument Set, is a reusable, steam sterilizable surgical instrument set consisting of a U-Channel…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Uromedica Inc.
FDA (openFDA device enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.