All recall categories

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 48,100 notices were distributed nationwide, so they reach California too — those are in the archive.

Medical devices

Reported Oct 5, 2022

MEDLINE CLEARPRO DOUBLE SWIVEL CLOSED SUCTION CATHETER, flat peel pouch EA, 10 EA per Inner Carton (IC), 20 EA/2 Inner…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

MEDLINE INDUSTRIES, LP - Northfield

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

MICRO-X ROVER MOBILE X-RAY SYSTEM, MXU-RV19

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Micro-X Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

OSSUR Power Knee REF PKA10003 OSSUR Power Knee REF PKA10003 OSSUR Power Knee REF PKA01001L OSSUR Power Knee REF…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ossur Americas

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

t:slim X2 insulin pump; t:slim X2 insulin pump with Dexcom G5; t:slim X2 insulin pump with Basal-IQ technology; t: slim…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Tandem Diabetes Care Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

Autosoft 90, model numbers 1000282, 1002817, 1002818, 1002819, 1002820, 1002821, 1002822, 1002823, and 1002824.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Unomedical A/S

FDA (openFDA device enforcement)

Food

Reported Oct 5, 2022

Dutch Red Potatoes with Dijon Mustard Sauce. NET WT. 1 LB 1.7 OZ (502g) UPC code 0-45255-15221-0 Distributed by World…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

World Variety Produce Inc. dba Melissa's

FDA (openFDA food enforcement)

Medical devices

Reported Sep 28, 2022

Fungitell STAT- IVD Assay for (1 ¿ 3)-~-D-Glucan in Serum Ref: FT007

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Associates

FDA (openFDA device enforcement)

Medical devices

Reported Sep 28, 2022

BD MaxGuard Extension Set with 4-way stopcock, REF: M4058

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Carefusion

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 28, 2022

AquaC UNO H [120V, 60Hz, 1000VA, US-Version - a reverse osmosis unit intended for use with hemodialysis systems.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Fresenius Medical Care Holdings, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 28, 2022

Golden Pacific California Shelled Almonds Sliced Almonds 25 LBS. NET WEIGHT Store away from heat Cold storage…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

J & N Nut Products Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 28, 2022

Grappler Suture Anchor, Titanium, 3.0 x 10mm, Sterile Kit, REF: P44-110-3010-SK, for use within the Grappler Suture…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Paragon 28, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 28, 2022

That's It. Dark Chocolate Banana Truffles Net WT. 3.5 oz, 5.0 oz, and 16.0 oz Ingredients: Organic Bananas, Organic…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

That's it. Nutrition, LCC

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 21, 2022

Roadrunner PC Hydrophilic Wire Guide REFERENCE PART NUMBER (RPN)RFPC-35-180 ORDER NUMBER (GPN) G07937. For vascular…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cook Incorporated

12 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 21, 2022

MicroClave Clear Neutral Connector. A bidirectional connector used as an accessory to an intravascular catheter placed…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ICU Medical, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 21, 2022

Pinnacle3 Radiation Therapy Planning System, Model numbers 870231 and 870237.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Drugs

Reported Sep 21, 2022

Bupivacaine HCl 0.375% w/v and Lidocaine HCl 2% w/v Solution for Retrobulbar or Peribulbar Injection; packaged in a) 10…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Pine Pharmaceuticals, LLC

FDA (openFDA drug enforcement)

Medical devices

Reported Sep 21, 2022

QIAcube Connect MDx, Model No. 9003070

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Qiagen Sciences LLC

FDA (openFDA device enforcement)

Medical devices

Reported Sep 21, 2022

Verify SixCess Challenge Pack. Used to confirm that critical parameters of steam sterilization have been reached within…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Steris Corporation Hopkins Facility

FDA (openFDA device enforcement)

Medical devices

Reported Sep 21, 2022

Disposable Subdermal Needle Electrode, Pt/lr, 12 x 0.40mm, product number TE/S46/638, 25 needles per package, sterile.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Technomed Europe

FDA (openFDA device enforcement)

Food

Reported Sep 21, 2022

The GFB Gluten Free Bites Dark Chocolate and Coconut 1.2oz. UPC 856818008895, 10 retail units per tray, 6 trays per…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

West Thomas Partners, LLC. dba Gluten Free Bar

FDA (openFDA food enforcement)

Medical devices

Reported Sep 14, 2022

Abbott Alinity m SARS-CoV-2 CTRL Kit, REF 09N78-085, each kit contains 12 x 1.3mL CTRL - and 12 x 1.3 mL CTRL +, For In…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Molecular, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 14, 2022

CARTO VIZIGO 8.5F Bi-Directional Guiding Sheath, REF: D138501. Used to introduce various cardiovascular catheters into…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Biosense Webster, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 14, 2022

Product Description/Item: ChemoLock Bag Spike, 10 units/CL-10-10; ChemoLock BAG SPIKE w/ ADDITIVE PORT, DRY…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ICU Medical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 14, 2022

Orthex External Fixation Wire Sharp Bayonet 1.8 x 400 mm Model: K400-18BN

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

OrthoPediatrics 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.