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 Mar 4, 2020
Ulrich medical neon3 OCT spinal stabilization, REF CS 3917-12, Locking screw for crosslink, screw-to-screw
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ulrich medical USA Inc.
FDA (openFDA device enforcement)
Reported Mar 4, 2020
THP Hip Plating System, Item Nos. 14-451070 14-451075 14-451080 14-451085 14-451090 14-451095 14-451100 14-451105…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
FDA (openFDA device enforcement)
Reported Mar 4, 2020
Zimmer Sterile Disposable Tourniquet Cuff with Protective Sleeve and PLC, Dual Port, Dual Bladder, Item No.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
FDA (openFDA device enforcement)
Reported Feb 26, 2020
Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-05400-CA1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
19 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 26, 2020
Don Lee Farms Chipotle Black Bean Burger 12 pack/3Lbs. cartons UPC 087427438135, Item 1372617 Don Lee Farms Chipotle…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Don Lee Farms
FDA (openFDA food enforcement)
Reported Feb 26, 2020
EDAN Telemetry Transmitter, Model iT20 - Product Usage: The iT20 telemetry transmitter is intended to be used in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edan Diagnostics
FDA (openFDA device enforcement)
Reported Feb 26, 2020
3/8" diced IQF zucchini in 45 pound poly lined carton
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hart Freeze Pack, LLC
FDA (openFDA food enforcement)
Reported Feb 26, 2020
UST-2265-2 Probe, Part Number: UST-2265-2 - Product Usage: The UST-2265-2 probe is intended to be used for diagnostic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported Feb 26, 2020
Medicrea International Universal Counter Torque for use with the Pass TULIP [Spinal] System Ref : A22020500
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medicrea International
FDA (openFDA device enforcement)
Reported Feb 26, 2020
DP-30 Digital Ultrasonic Diagnostic Imaging System, Part No. 1155E-PA00004 - Product Usage: The Digital Ultrasonic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mindray DS USA, Inc. dba Mindray North America
FDA (openFDA device enforcement)
Reported Feb 26, 2020
Guided Start Drills/Counterbore NobRpl NP - Product Usage: The Guided Drills (Twist (Step) Drills, Guided Tapered…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nobel Biocare USA LLC
23 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 26, 2020
SnapLink, Ref Part No. 438-2190, L6R SnapLink, Slot .022, TQ--28, Ang +2, Rot +2, Qty 10, Made in Mexico, CE 0086, Rx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ormco/Sybronendo
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 26, 2020
CombiDiagnost GCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray system, diagnostic, fluoroscopic,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems GmbH, DMC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 26, 2020
Philips HeartStart FRx AED, Model 861304, FRx codeRev: E.02.017
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 Feb 26, 2020
TwinFix Ti 2.8 mm HS Suture Anchor - Product Usage: A fixation device intended to provide secure attachment of soft…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (openFDA device enforcement)
Reported Feb 26, 2020
Suja Organic Berry Zest Fruit + Veggie Smoothie, 12 oz. UPC: 81861702234
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Suja Life LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 26, 2020
OPTILITE IgM Kit, REF: NK012.OPT.A, IVD, UDI: 05051700017565
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Binding Site Group, Ltd.
FDA (openFDA device enforcement)
Reported Feb 19, 2020
FlexTip Plus Combined Spinal Epidural Catheterization Set, Product Code AA-05400-B
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
48 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 19, 2020
Blue Ortho TKA Pro v2.1 software installed on the Exactech GPS system -indicated for stereotaxic surgery in Knee…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Blue Ortho
FDA (openFDA device enforcement)
Reported Feb 19, 2020
LivaNova Sorin Connect DPIII KOMPL. S5 REF 96-415-130, 2017-08-15, IPX1, RXOnly, (01)04033817901594 Product Usage: The…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Feb 19, 2020
bliss anti-stress formula Dietary Supplement, 60 Tablets; Manufactured For and distributed by: Market America, Inc.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Market America Inc.
FDA (openFDA food enforcement)
Reported Feb 19, 2020
Medtronic MiniMed 630G System with SmartGuard, Ref/Model # MMT-1515, MMT-1715, MMT-1714, MMT-1754, and MMT-1755 *US and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 19, 2020
Stratum Lapidus Plate - Small Rt, Part No. STRM-LAP-SMR, UDI 00817701025467. The product is part of the Stratum Foot…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nextremity Solutions
FDA (openFDA device enforcement)
Reported Feb 19, 2020
Button-Style Tocotransducer (Nautilus), 8-foot Cord 2264HAX, that may have been serviced with the following: Pacific…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pacific Medical Group Inc.
9 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.