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.
7,509 stored notices name California, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,842 notices were distributed nationwide, so they reach California too — those are in the archive.
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)
Reported May 6, 2020
ViewRay System: Model No. 10000 and 20000 for radiation treatment. PN11440 MRIdian System Treatment Planning and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Viewray, Inc.
FDA (openFDA device enforcement)
Reported May 6, 2020
Lead diagnostic electrocardiograph under the following device names: ELI 10, ELI 350, ELI 150c, ELI 250c, ELI 230, ELI…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Welch Allyn, Inc/mortara
9 more products in this recall
FDA (openFDA device enforcement)
Reported May 6, 2020
Whole Foods Market Minestrone Soup PLU code printed on the product scale labels beginning with 248529 for soup sold in…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Whole Foods Market
FDA (openFDA food enforcement)
Reported Apr 29, 2020
ARCHITECT HAVAB G Reagent Kit. List Number 6L27 25.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott GmbH & Co. KG
FDA (openFDA device enforcement)
Reported Apr 29, 2020
Rhythm Xience Guider Catheter Introducer with Lancer Intergrated Dilator/Transseptal Needle, Ref 112852, Sterile EO,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acutus Medical Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 29, 2020
Beckman Coulter Power Express Sample Processing System AU5800XL connection unit, catalog #B36351; and Power Express…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 29, 2020
Fentanyl Reagent Kit, Product N. CC444, Contains: FENT R1 Reagent and FENT R2 Reagent
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carolina Liquid Chemistries Corp.
FDA (openFDA device enforcement)
Reported Apr 29, 2020
Lake Champlain CHOCOLATES, COIN DARK BULK ORG, NET WT 48 OZ (1.3 kg), APPROX 186 PIECES, INGREDIENTS: DARK CHOCOLATE…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Champlain Chocolate Company
FDA (openFDA food enforcement)
Reported Apr 29, 2020
TCM4 Base unit, Ref 391-880, UDI:(01)05700693918808, used with the monitor modules TCM4 (902-778), TCM40 (902-778,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 29, 2020
Smith & Nephew FOOTPRINT ULTRA PK SUTURE ANCHOR 4.5 Part Number: 72202901
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 22, 2020
Merlin PCS 3650 Software Upgrade Kit, REF 3330 St. Jude Medical The MerlinTM Patient Care System (MerlinTM PCS) Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott
FDA (openFDA device enforcement)
Reported Apr 22, 2020
Nitinol Thermocouple Electrode, 10 cm - Product Usage: The TCN Electrode is indicated for use in RF heat lesioning of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Neuromodulation Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 22, 2020
Canon Aquilion Lightning, Model TSX-036A
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
7 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 22, 2020
SPICE (JWH-018) CC443
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carolina Liquid Chemistries Corp.
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.