Recalls distributed in New Jersey
These notices name New Jersey 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.
4,822 stored notices name New Jersey, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach New Jersey too — those are in the archive.
Reported Dec 30, 2020
42 IN (107 cm) Appx 5.0 ml, 20 Drop Admin Set, Spiros, REF: 20131-01; 31" (79 cm) Admin Set w/20 Drop Integrated Clave…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 30, 2020
CACAO MARKET MARIE BELLE NEW YORK; Dark Chocolate Pearls; Ingredients: Cocoa bean, sugar, biscuit cereals (wheat flour,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Maribel's Sweets, Inc.
FDA (openFDA food enforcement)
Reported Dec 30, 2020
Star 8 Rolling Walker/Rollator, Items: 4258/ BK(Black)/ BL(Blue)/ DB(Sky Blue)/ PL(Purple)/ RD(Red)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nova Ortho-Med Inc.
FDA (openFDA device enforcement)
Reported Dec 23, 2020
BD PrecisionGlide Needle 30G x 1/2 (0.3 mm X 13mm) REF 305106 - Product Usage: used for general purpose injection and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Dec 23, 2020
Carl Zeiss Meditec Ag VISULENS 550 REF 2268-038 - Product Usage: is a device for measuring the refractive power of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carl Zeiss Meditec AG
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 23, 2020
Centeze Centesis Catheter, 6F, 10cm, 18Ga, 12cm, REF DRC-002-06 Centeze Centesis Catheter, 6F, 10cm, 18Ga, 12cm, REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Galt Medical Corporation
FDA (openFDA device enforcement)
Reported Dec 23, 2020
K-ACT Actalyke Clotting Test Tubes that are used in the: ACTALYKE XL ACTIVATED CLOTTING TIME ANALYZER, and ACTALYKE…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Helena Laboratories, Corp.
FDA (openFDA device enforcement)
Reported Dec 23, 2020
Tina-quant C-Reactive Protein Gen.3, Catalog number 05172373190 - Product Usage: the in vitro quantitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Dec 16, 2020
BD" Multi-Check CD4 Low Control 2.5 mL IVD - Product Usage: intended as a complete process control for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company, BD Biosciences
FDA (openFDA device enforcement)
Reported Dec 16, 2020
MAC VU360, Electrocardiograph
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Dec 16, 2020
Golden Boy brand Custard muffin Original; 7.76 ounce, rigid clear plastic packages
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hong Thai Foods Corp.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 16, 2020
On the Go Sweet & Salty Trail Mix
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kanan Enterprises Inc.
FDA (openFDA food enforcement)
Reported Dec 16, 2020
Randox Mg R1 - Product Usage: For the quantitative in vitro determination of Magnesium in serum, plasma and urine…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 16, 2020
Shimadzu Mobile X-Ray System, MobileDaRt Evolution (MX8 Version), with adjustable handle option, Made in Japan -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Medical Systems
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 16, 2020
Sentinel V10.x & V11.x, Models: 98200 & 98201 - Product Usage: designed using the latest programming technology and is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare, Ltd.
FDA (openFDA device enforcement)
Reported Dec 16, 2020
PROKERA, non-sterile - Product Usage: Biologic corneal bandage.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TissueTech, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 16, 2020
1. Fresh Attitude Baby Spinach, 11 oz. 2. Fresh Attitude Baby Spinach, 5 oz.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Veg Pro International Inc.
FDA (openFDA food enforcement)
Reported Dec 9, 2020
YAGUMO AMANATTO GIFT BOX 6P 6/19.01 OZ JAN Code: 49 03089 39050 4 Imported by JFC International Inc. Los Angeles, CA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.J F C International Inc.
FDA (openFDA food enforcement)
Reported Dec 9, 2020
B. Braun Introcan Safety IV Catheters, Product codes REF 4252500-01 4252519-01 4252535-01 4252560-01 4252586-01…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Janus Trade Group
FDA (openFDA device enforcement)
Reported Dec 9, 2020
Quantum Health branded Elderberry liquid herbal extract dietary supplement is packaged in 2oz glass bottle, 12…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Quantum Inc.
FDA (openFDA food enforcement)
Reported Dec 9, 2020
BladderScan Prime Plus Probe REF 0570-0395 - Product Usage: intended to be used for measuring the urine volume in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Verathon, Inc.
FDA (openFDA device enforcement)
Reported Dec 2, 2020
Titan Pump - Product Usage: indicated for male patients suffering from erectile dysfunction (impotence) who are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Coloplast Manufacturing US, LLC
FDA (openFDA device enforcement)
Reported Dec 2, 2020
Synergy raw kombucha - Multi-Green; 16 fl. oz. (473 mL) UPC 7 22430 14016 2 GT's Living Foods LLC Beverly Hills, CA
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GT's Living Foods
FDA (openFDA food enforcement)
Reported Dec 2, 2020
Box Label: ION Fully Articulating Catheter, REF 490105, VER 08 - Product Usage: used to navigate the Ion Fully…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, 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.