State

New Jersey product recalls

73,598 recalls have nationwide distribution and so reach New Jersey. 9,773 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total: 9,773
Critical: 1,246
Severe: 2,942
Most recent: 2026-10-14

Of the 9,773 recalls naming New Jersey we have scored against our rubric, 1,246 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,942 (30%) are Severe.

Which agencies issued them

These figures cover only the 9,773 recalls whose distribution notice names New Jersey specifically. The 73,598 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28326–28350 of 83371

HighFDA (Devices)·Z-1653-2021·2021-05-26
Bard Groshong NXT ClearVue Catheter Recall for Connector Defects
Bard Access Systems is recalling Groshong NXT ClearVue Catheters because connector defects may prevent proper catheter passage or locking.
Product
REF 7617405J, Groshong NXT ClearVue Catheter, Basic kit, 4F, Single-Lumen, 60 cm, UDI: (01)10801741200592 - Product Usage: is designed for use when central venous catheterization is prescribed.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V393000·2021-05-26
Grand Design RV Travel Trailers LP Regulator Fire Risk Recall
Grand Design is recalling 55,508 travel trailers (2016-2021 Imagine, Transcend, Momentum) for defective LP regulators that may cause excessive gas pressure and increase fire risk. Free replacement available through dealers.
Product
GRAND DESIGN — GRAND DESIGN IMAGINE, MOMENTUM, TRANSCEND
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1632-2021·2021-05-26
Biopsybell Recalls Sterile Spine Bone Filler Due to Sterilization Concerns
Biopsybell S.R.L. is recalling 60 units of Renova Spine Bone Filler labeled as sterile but potentially not sterilized. The product was distributed in Mississippi and Kentucky.
Product
RENOVA SPINE BONE FILLER 10G 12CM CENTIM. STERILE, RESFIL1112C1-US
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1645-2021·2021-05-26
Biopsybell 8G Direct Working Cannula Bevel Tip Recalled for Sterility Concerns
Biopsybell S.R.L. is recalling 8G Direct Working Cannula Bevel Tips labeled as sterile but potentially not sterilized. The recall affects 30 units distributed in Mississippi and Kentucky.
Product
8G DIRECT WORKING CANNULA BEVEL TIP, CODE INTV-DWCB
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V391000·2021-05-26
Heavy-duty trucks recalled for fuel rail defect and fire risk
PACCAR is recalling certain 2018-2021 Kenworth and Peterbilt commercial trucks because a sealing washer defect in the fuel rail assembly may cause fuel leaks. When fuel leaks occur near an ignition source, fire risk increases.
Product
PETERBILT — PETERBILT, KENWORTH 367, 337, 567, T370
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1662-2021·2021-05-26
Bard Access Systems Recalls Groshong NXT ClearVue Catheters Due to Connector Defects
Bard Access Systems is recalling specific lots of Groshong NXT ClearVue Catheters because connector defects may prevent proper catheter passage or locking.
Product
REF 9617408D, Groshong NXT ClearVue Catheter with Sherlock Tip Location System (TLS) Stylet, Maximal Barrier Kit, 4F, Single-Lumen, TLS, UDI: (01)10801741036016 - Product Usage: is designed for use when central venous catheterization is prescribed.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1664-2021·2021-05-26
Bard Access Systems Recalls Groshong NXT ClearVue Catheters Due to Connector Defects
Bard Access Systems is recalling specific lots of Groshong NXT ClearVue Catheters because connector defects may prevent proper catheter passage or locking.
Product
REF 69655405, Groshong NXT ClearVue Catheter with Sherlock Tip Location System (TLS) Stylet, Basic Kit, 4F, Single-Lumen, TLS, UDI: (01)10801741147521 - Product Usage: is designed for use when central venous catheterization is prescribed.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1661-2021·2021-05-26
Bard Groshong NXT ClearVue Catheter Recall for Connector Defects
Bard Access Systems is recalling Groshong NXT ClearVue Catheters due to defects in the distal connector that may prevent proper catheter passage or locking.
Product
REF 9617408, Groshong NXT ClearVue Catheter with Sherlock Tip Location System (TLS) Stylet, Full Kit, 4F, Single-Lumen, TLS, UDI: (01)10801741036009 - Product Usage: is designed for use when central venous catheterization is prescribed.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0542-2021·2021-05-26
Bloommy Biotin Collagen Keratin Capsules Recalled for Undeclared Fish
Bloommy Inc. is recalling Biotin Collagen Keratin Capsules because they contain undeclared fish collagen, a potential allergen.
Product
"Bloomy*** Biotin Collagen Keratin***Capsules for SKIN, JOINT, HAIR***Supplement Facts***Marine Collagen***Manufactured for Bloommy Inc. 106 W. Broad St. Pawcatuck, CT 06379"
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1655-2021·2021-05-26
Bard Groshong Catheter Recall for Connector Defects
Bard Access Systems is recalling specific lots of Groshong NXT ClearVue Catheters due to connector defects that may prevent proper catheter passage or locking.
Product
REF 7617408D, Groshong NXT ClearVue Catheter, Maximal Barrier Kit, 4F, Single-Lumen, 60 cm, UDI: (01)10801741035262 - Product Usage: is designed for use when central venous catheterization is prescribed.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V397000·2021-05-26
2021 KZRV SPORTTREK and STRATUS trailers water heater circuit fire hazard
KZRV is recalling 2021 SPORTTREK and STRATUS trailers with incorrectly sized water heater circuit breakers. The wiring defect may prevent proper electrical protection and increase fire risk.
Product
KZRV — KZRV SPORTTREK, STRATUS
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·21141·2021-05-26
Target Recalls Room Essentials Shower Stools Due to Fall Hazard
Target is recalling Room Essentials Shower Stools because they can become unstable or slippery, posing a fall hazard. About 58,500 units were sold.
Product
Room Essentials Shower Stools
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1596-2021·2021-05-26
Roche Recalls Troponin I Immunoassay Kits Due to False Negative Risk
Roche Diagnostics is recalling 726 Elecsys Troponin I Immunoassay kits because they may produce false negative results when run immediately after proBNP II tests on specific modules.
Product
Elecsys Troponin I Immunoassay: Catalog# 05094810160 - Product Usage: intended to aid in the diagnosis of myocardial infarction.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21139·2021-05-26
Ergobaby Recalls METROUS Strollers Due to Choking Hazard
Ergobaby is recalling METROUS strollers because a harness buckle button can break and detach, posing a choking hazard to young children.
Product
METROUS1, METROUS2 and METROUS4 Compact City Strollers
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1669-2021·2021-05-26
Bard Groshong NXT ClearVue Catheter Recall for Connector Defects
Bard Access Systems is recalling specific lots of Groshong NXT ClearVue Catheters due to connector defects that may prevent proper catheter passage or locking.
Product
REF 7617407, Groshong NXT ClearVue Catheter, Full Kit, 4F, Single-Lumen, 60 cm, UDI: (01)10801741035248 - Product Usage: is designed for use when central venous catheterization is prescribed.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0537-2021·2021-05-26
PepsiCo Recalls Evolve Protein Shakes Due to Undeclared Soy
PepsiCo is recalling Evolve Double Chocolate Plant-Based Protein Shakes because they contain undeclared soy. The recall covers 17,381 cases distributed nationwide.
Product
Evolve Double Chocolate Plant-Based Protein Shake, 11oz "Tetra Pak" carton, sold 4 cartons per retail unit. UPC on retail 4 pack: 876063007887 Packed 3 retail four packs per wholesale case.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1646-2021·2021-05-26
Biopsybell Cement Delivery Kits Recalled for Potential Sterility Failure
Biopsybell is recalling 305 units of 10 Gauge Single Cement Delivery kits because they were labeled sterile but may not have been sterilized.
Product
10 GAUGE SINGLE CEMENT DELIVERY 4 FILLERS 4 SYRINGES, CODE INTVM-SCDK
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1666-2021·2021-05-26
Bard Groshong NXT ClearVue Catheter Recall for Connector Defects
Bard Access Systems is recalling specific Groshong NXT ClearVue Catheters because connector defects may prevent proper catheter passage or locking.
Product
REF CK000379, Groshong NXT ClearVue Catheter with Sherlock Tip Location System (TLS) Stylet, Full Kit, 4F, Single-Lumen, TLS, CE 2797, UDI: (01)10801741102704 - Product Usage: is designed for use when central venous catheterization is prescribed.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1657-2021·2021-05-26
Bard Groshong NXT ClearVue Catheter Recalled for Connector Defects
Bard Access Systems is recalling Groshong NXT ClearVue Catheters because connector defects may prevent proper catheter passage or locking.
Product
REF 7655405J, Groshong NXT ClearVue Catheter, Basic Kit, 4F, Single-Lumen, 60 cm, UDI: (01)10801741200615 - Product Usage: is designed for use when central venous catheterization is prescribed.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1667-2021·2021-05-26
Bard Access Systems Recalls Groshong NXT ClearVue Catheters Due to Connector Defects
Bard Access Systems is recalling specific lots of Groshong NXT ClearVue Catheters because connector defects may prevent proper catheter passage or locking.
Product
REF CK000516, Groshong NXT ClearVue Catheter with Sherlock 3CG Tip Positioning System (TPS) Stylet, Full Kit, 4F, Single-Lumen, TPS, CE 2797, UDI: (01)10801741107891 - Product Usage: is designed for use when central venous catheterization is prescribed.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V395000·2021-05-26
2017–2021 Holiday Rambler and Fleetwood Motorhomes Recalled for Improperly Sealed Flooring
REV Recreation Group is recalling 2017–2021 Fleetwood, Holiday Rambler, and Fleetwood motorhomes with improperly sealed floor holes that could allow carbon monoxide into the living area. Dealers will reseal the floor free of charge.
Product
HOLIDAY RAMBLER — HOLIDAY RAMBLER, FLEETWOOD VACATIONER, BOUNDER, SOUTHWIND
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0494-2021·2021-05-26
Public Goods Hair, Skin, & Nails Supplement Recalled for Undeclared Soy
Public Goods is recalling Hair, Skin, & Nails dietary supplements because they may contain undeclared soy. Consumers with soy allergies should stop using the product.
Product
PUBLIC GOODS brand HAIR, SKIN, & NAILS Dietary Supplement; 60 tablets per bottle; Other ingredients: Stearic acid; croscarmellose sodium, magnesium stearate, aqueous film coating (purified water, hydroxypropyl methylcellulose, vegetable glycerin), microcrystalline cellulose.…
Category
Food
Distribution
51 states
HighNHTSA·21V394000·2021-05-26
Pierce Recalls 2017-2021 Commercial Vehicles Due to Fuel Rail Leak Risk
Pierce Manufacturing is recalling 2017-2021 Arrow XT, Enforcer, Impel, Quantum, Saber, and Velocity vehicles because a sealing washer defect may cause high-pressure fuel leaks, increasing fire risk.
Product
PIERCE — PIERCE ARROW XT, ENFORCER, VELOCITY, IMPEL
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1650-2021·2021-05-26
Medtronic Recalls Two Defective Implantable Cardioverter Defibrillators
Medtronic is recalling two Cobalt HF Quad MRI SureScan CRT-D devices due to a potential missing resistance spot weld.
Product
Cobalt HF Quad MRI SureScan Implantable Cardioverter Defibrillators with Cardiac Resynchronization Therapy (CRT-D) - Product Usage: are multiprogrammable cardiac devices that monitor and regulate a patient s heart rate by providing single- or dual chamber rate responsive…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1595-2021·2021-05-26
Roche Recalls Troponin I STAT Immunoassay Kits Due to False Negative Risk
Roche Diagnostics is recalling 10,489 Troponin I STAT Immunoassay kits because they may produce false negative results when run after proBNP II tests on specific modules.
Product
Elecsys Troponin I STAT Immunoassay: Catalog# 05094798160 - Product Usage: intended to aid in the diagnosis of myocardial infarction.
Category
Medical Device
Distribution
Distributed nationwide