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 48,828 notices were distributed nationwide, so they reach California too — those are in the archive.
Reported Jul 22, 2020
WinCo Foods Tater Bites Shaped, Shredded Potatoes, frozen product. Retail 32 oz. poly bag has UPC 0 70552 30303 4. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lamb Weston Inc.
FDA (openFDA food enforcement)
Reported Jul 22, 2020
DRW-0739-01: Gen 2 Posterior Chairside Splint LLUR (lower left-upper right) - Product Usage: intended to provide…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Neocis Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 22, 2020
ACUMED CALLOS INJECT 10CC. Product Number: 65-0010-S, UDI: 813845020245 - Product Usage: Callos is indicated to fill…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Skeletal Kinetics, LLC
44 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 22, 2020
Whole Foods Market Red Velvet Layered Cheesecake Slice PLU: 78620 packaged in plastic clam shell with scale label…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Whole Foods Market
FDA (openFDA food enforcement)
Reported Jul 15, 2020
The CapsoCam Plus (SV-3); Device Common Name: System, Imaging, Gastrointestinal, Wireless, Capsule; Catalog Number 2795…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Capso Vision, Inc.
FDA (openFDA device enforcement)
Reported Jul 15, 2020
FHC Guideline 4000 5.0 GL5 Main Processing Unit - Product Usage: intended to record and stimulate electrophysiological…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.FHC, Inc.
FDA (openFDA device enforcement)
Reported Jul 15, 2020
Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes. Sterile and single use only. Catalog number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kentec Medical, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 15, 2020
Extra corporeal circuit with bio-active surface.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
FDA (openFDA device enforcement)
Reported Jul 15, 2020
EasyDiagnost Eleva DRF, model no. 706050 - Product Usage: X-ray system, diagnostic, general-purpose.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 15, 2020
Blanxart 85% Nicaragua Organic Dark Chocolate Bar, packaged in paper packaging with internal foil wrapper. Net weight…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Power Selles Imports dba Culinary Collective
FDA (openFDA food enforcement)
Reported Jul 15, 2020
DABRA Laser (RA-308 Excimer Laser). The DABRA Laser and DABRA Catheter is an excimer laser ultraviolet light source and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ra Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jul 15, 2020
Blood gases (PCO2, PO2) and blood pH test system; ABL800 FLEX; Model Number 393-800; UDI (01)05700693938004. Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 15, 2020
3COR DISTRACTION SCREW, 12 MM, STERILE, 5/BOX - Product Usage: intended to be used for distraction in the anterior…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TeDan Surgical Innovations LLC
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 15, 2020
TOMTEC-ARENA TTA2;software version no. 2.20 and lower; Picture archiving and communications system. Software Versions…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tomtec Imaging Systems GmbH
FDA (openFDA device enforcement)
Reported Jul 8, 2020
Flow Coupler Monitor, GEM, Global Excellence Microsurgery, Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Jul 8, 2020
CODAN SWAN-LOCK Swabable Needlefree Connector, Catalog #BC1000N, REF 16.7220, individually packaged, 504/case, Sterile.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Codan US Corporation
FDA (openFDA device enforcement)
Reported Jul 8, 2020
NORTH STAR TRADING COMPANY SWEET & SALTY CARAMEL TRAIL MIX NET WT 14OZ (396g) MANUFACTURED FOR YOUR MILITARY EXCHANGES…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Flagstone Foods LLC
FDA (openFDA food enforcement)
Reported Jul 8, 2020
Sterile Disposable Connectors ASY CONN Y 1/2X1/2X3/8 STR 24. REF/ GTIN for Insert Label:029165000/ 00803622123153
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
21 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2020
VITROS 3600 Immunodiagnostic System Software Versions 3.3.3 and below Product Code: 6802783, Unique Identifier:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho Clinical Diagnostics
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2020
Maestro Orthodontic Bracket REF711-206-10 QTY. 10 Rx Only (01)00190707016517 (10)112233 (422)484
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho Organizers, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2020
ABL80-FLEX-393-839 Box Label, REF 393-839, IVD, CE, UDI: 05700693938394 - Product Usage: It is intended for use in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2020
Siemens IMMULITE 2000 Immunoassay System - In vitro Chemistry Analyzer SMN #10380062 - Product Usage: are intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2020
TOUFAYAN BAKERIES SMART POCKETS EVERYTHING 6 COUNT NET WT 7.4 OZ. (210 g), UPC 0 7312400792 7. 12 packages per case.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Toufayan Bakery, Inc.
FDA (openFDA food enforcement)
Reported Jul 8, 2020
Neo-Vent Infant T-Piece Resuscitation Circuit;Circuit for use on compatible Infant Resuscitators. 15mm OD x 10mm ID…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Westmed, Inc.
2 more products in this recall
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.