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 48,100 notices were distributed nationwide, so they reach New Jersey too — those are in the archive.
Reported Dec 4, 2024
Essenz HLM (Heart-Lung Machine), REF: 49-00-10, with Software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova Deutschland GmbH
FDA (openFDA device enforcement)
Reported Dec 4, 2024
Autosampler, Models: SIL-20ACXR CL, SIL-20ACHT CL, SIL-30AC CL
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Corp. Analytical & Measuring Instruments Div.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 4, 2024
Brand Name: Z-800 Infusion System Product Name: Z-800WF Model/Catalog Number: Z-800WF. The Z-800 Infusion system is…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Zyno Medical LLC
FDA (openFDA device enforcement)
Reported Nov 27, 2024
Bard Marquee Disposable Core Biopsy Instrument Kit: BARD MARQUEE KIT 12G X 10 CM, REF: MQK1210; BARD MARQUEE 12G X 10…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Nov 27, 2024
EnChroma Safety Glasses with Rx Indoor Universal Lenses: Martinez Cx1 Indoor Rx, SKU: Cx.PC.IN.MTZ.BK.Rx; Summit Indoor…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Enchroma Inc.
FDA (openFDA device enforcement)
Reported Nov 27, 2024
MONOCRYL" (poliglecaprone 25) Suture REF Y936H MONOCRYL" Sutures are indicated for use in general soft tissue…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon, Inc.
FDA (openFDA device enforcement)
Reported Nov 27, 2024
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4720
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hobbs Medical, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2024
BELEVINI, DRIED FRUIT MIX (Apples, Pears & Plums w/pit), 500g, PLASTIC SOFT PACK, 6 PACKAGES PER CASE
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MAMTAKIM, Inc.
FDA (openFDA food enforcement)
Reported Nov 27, 2024
Douglas Labs Stress-B-Plus Dietary Supplement, Tablets, 90 tablets per bottle. UPC # 10539 97452, Lot Numbers ,50335944…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nestle Product Technology Center - Nestle Health Science
FDA (openFDA food enforcement)
Reported Nov 27, 2024
cobas HCYS, Homocysteine Enzymatic Assay, Material Number REF 06542921190, for use on cobas c 701/702, in vitro test…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Nov 27, 2024
Aldi Emporium Selection Brie 8oz UPC 4099100084016; 12 retail units per case La Bonne Vie Brie 8oz UPC 820581678531; 6…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Savencia Cheese USA
2 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 20, 2024
The EVSRF catheter is a sterile, single-use disposable medical device for endovenous radiofrequency ablation, a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Nov 20, 2024
Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Software Version: Not applicable Component:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 20, 2024
Medtronic Recharger Kits, RS6230, RS7230, and RS5220A, containing components WR9230 and WR9220A Recharger for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Nov 20, 2024
Brand Name: Olympus Product Name: Cystoscope Outer Sheath Model/Catalog Number: WA22810A Software Version: N/A Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2024
Elekta Disposable Biopsy Needle Kit for Leksell Stereotactic System, REF 911933, Diameter / 14 Gauge, containing 6…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Elekta Instrument AB
FDA (openFDA device enforcement)
Reported Nov 13, 2024
Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 5mL bottles, Rx only, Manufactured by: FDC Limited, Waluj,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.FDC Limited
FDA (openFDA drug enforcement)
Reported Nov 13, 2024
Hammond's Dark Chocolate Filled Mini Waffle Cones, packaged in a 4 oz (113g) Stand-Up Resealable Pouch. Item Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hammond's Candies Since 1920 II, LLC
FDA (openFDA food enforcement)
Reported Nov 13, 2024
Medtronic DLP Aortic Root Cannula with Flow-Guard, REF 11012; for use in cardiopulmonary bypass surgery
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
FDA (openFDA device enforcement)
Reported Nov 6, 2024
Abbott Alinity m HPV AMP Kit, used with the Alinity m System, product codes: a) REF 09N15-095; b) REF 09N15-090; c) REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Molecular, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 6, 2024
(Principal Display) ENOKI MUSHROOM Champignons d'enoki Net Wt: 150g (5.3oz) in a clear plastic packaged. (Back Display)…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Enoki King Mushroom Farm Inc.
FDA (openFDA food enforcement)
Reported Nov 6, 2024
ClariTEE Probe- Miniature transesophageal echo ultrasound probe for use with ImaCor ultrasound diagnostic platforms.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ImaCor Inc.
FDA (openFDA device enforcement)
Reported Nov 6, 2024
Phasitron5 Breathing Circuit (P5-10, P5-HC, P5-UC-10). component of Intrapulmonary Percussive Ventilation, used to…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Percussionaire Corporation
FDA (openFDA device enforcement)
Reported Nov 6, 2024
Sprouts Chicken Street Taco, 6 taco, perishable item kept under refrigeration, packaged in a plastic tray with plastic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sprouts Farmers Market
FDA (openFDA food 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.