All recall categories

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.

4,754 stored notices name New Jersey, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,132 notices were distributed nationwide, so they reach New Jersey too — those are in the archive.

Medical devices

Reported Dec 24, 2014

RESTORIS PST Straight Shell Inserter An impactor is a reusable instrument designed for use by orthopedic surgeons…

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

Mako Surgical Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 24, 2014

SOLGAR ENHANCED SERIES ABC DOPHILUS POWDER FOR INFANTS AND CHILDREN, NET WT. 1.75 oz (50 g), UPC 0 33984 00010 0.…

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

NBTY, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 24, 2014

Additional devices identified in new FSN MA-FCO 83000190: QLAB versions 10.0 with a2DQ and/or aCMQ plug-ins installed…

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

Philips Ultrasound, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 24, 2014

Specialty Audible Torque Wrench Mfg by: Stryker Spine, Catalog number IS3002XLP, Non-sterile. Used to final tighten to…

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

Stryker Spine

FDA (openFDA device enforcement)

Food

Reported Dec 24, 2014

Wegmans Peach Salsa, made fresh in-store and packaged in random weights.

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

Wegmans Food Markets, Inc.

9 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 17, 2014

HeartLight Seafood brand Frozen Yellowfin Tuna Ground Meat (Thunnus albacares), IQF packed in a master carton of 10 x 1…

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

Heartlight Seafood LLC

FDA (openFDA food enforcement)

Medical devices

Reported Dec 17, 2014

Invacare Perfecto 2 V Oxygen Concentrator The finished device is packaged as a single unit. The service part contains a…

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

Invacare Corporation

FDA (openFDA device enforcement)

Food

Reported Dec 17, 2014

Chicken flavored broth base and seasoning, low sodium sold under the Orrington Farms brand in 5 oz. plastic jars.

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

Kent Precision Foods Group, Inc.

FDA (openFDA food enforcement)

Food

Reported Dec 17, 2014

Margaret Holmes Mixed Greens 14.5 oz, Distributed by McCall Farms, Effingham, SC

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

Mccall Farms Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 17, 2014

BrightView XCT is a gamma camera for Single Photon Emission Computed Tomography (SPECT) and integrates with an…

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

Philips Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 17, 2014

Align Radial Stems, Prosthesis, Elbow, Hemi Replacement of the radial head for degenerative or post-traumatic…

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

Skeletal Dynamics

FDA (openFDA device enforcement)

Medical devices

Reported Dec 17, 2014

Crocodile (size 3) are two-armed, wheeled walking aids, used by children with disabilities. Product Usage: The…

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

Snug Seat Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 10, 2014

Amerigel Hydrogel Wound Dressing Wound management

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

Amerx Health Care Corp.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 10, 2014

MAS CardioImmune XL Cardiac Marker Control; Model: CAI-XL1; intended for use in the clinical laboratory as an assayed…

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

Microgenics Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 10, 2014

Aquapak Adaptor, 028 NEB, INTL, Product No. 403128; Aquapak Adaptor, 033 NEB, INTL, Product No. 403133; Aqaupak…

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

Teleflex Medical

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2014

ARCHITECT Total T3 Reagent Kit (7K64) consists of: - 1 or 4 Bottle(s) (6.6 mL/27.0 mL) anti-T3 (sheep) coated…

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

Abbott Ireland Diagnostics Division

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2014

Cannulaide, Model 101, 102, 103. Respirator. The Cannulaide product is composed of die-cut hydrocolloid-coated…

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

Beevers Manufacturing & Supply, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2014

Calcitonin ELISA Kit, Code No. 7024, 7024BU. Intended use of this product is the quantitative determination of…

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

Biomerica

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2014

BrightView product code: 882478 BrightView X product code: 882480 BrightView XCT product code: 882482 and 882454

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

Philips Medical Systems (Cleveland) Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 3, 2014

Frozen Raw Yellowfin Tuna Ground Meat (Thunnus albacares), Grade: AAA, Net Weight: 10 lbs (100%), Wild Caught, Product…

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

Sushi House Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 3, 2014

Trabecular Metal Tibial Impactor. Product Usage: TM Tibial Impactor pads are used in conjunction with the TM Tibial…

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

Zimmer, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2014

CyberKnife Robotic Radiosurgery System with the first generation IRIS Variable Aperture Collimator. The CyberKnife is…

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

Accuray Incorporated

FDA (openFDA device enforcement)

Food

Reported Nov 26, 2014

GOLDEN LION brand DRIED ZIZIPHUS JUJUBA MILL (DRIED DATES), NET WT. 12 oz (340 g), UPC 7 34765 04008 6 -- PRODUCT OF…

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

Blooming Import Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 26, 2014

Edwards Lifesciences Vent Catheters, . Packaged sterile and non-pyrogenic in a sealed, peel-type pouch. Model Numbers:…

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

Edwards Lifesciences, LLC

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.