State

New Jersey product recalls

72,966 recalls have nationwide distribution and so reach New Jersey. 9,760 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total: 9,760
Critical: 1,249
Severe: 2,483
Most recent: 2026-09-16

Of the 9,760 recalls naming New Jersey we have scored against our rubric, 1,249 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,483 (25%) are Severe.

Which agencies issued them

These figures cover only the 9,760 recalls whose distribution notice names New Jersey specifically. The 72,966 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5151–5175 of 82726

HighFDA (Devices)·Z-0176-2026·2025-10-22
Cardiovascular procedure packs recalled after being sterilized more than once
American Contract Systems is recalling cardiovascular convenience kits that were re-gassed after a sterilization nonconformance, without validation for multiple cycles.
Product
Medical convenience kits Item Number/Description ANCV78BC HEART PACK - 205947 HGCV05K CV SET UP PACK MHPP97AR PACEMAKER PACK- 206010 UDBH37AW BASIC HEART PACK - 206044 UHPP82AH PERIPHERAL PACK - 209533 UICD62AN CARDIOVASCUALR SUPPLY (PS 907285) UICT16F CARDIO THORACIC
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0184-2026·2025-10-22
Orthopedic procedure packs recalled after being sterilized more than once
American Contract Systems is recalling shoulder, hip and extremity convenience kits that were re-gassed after a sterilization nonconformance, without validation for multiple cycles.
Product
Medical convenience kits Item Number/Description ANSH14AF SHOULDER PACK - 205962 EVAH76H ANTERIOR HIP PACK FDSA15M SHOULDER ARTHROSCOPY GRTS90G TOTAL SHPULDER PACK HGHI26G HIP PINNING PACK HJTO25C TOTAL HIP ACCESSORY PACK HNEX60L EXTREMITY PACK IAHD53C HAND PACK IAS
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0191-2026·2025-10-22
Non-vented IV solution sets recalled from one lot because sets may leak
Baxter is recalling 1,440 CLEARLINK System non-vented solution sets from one lot because the IV sets may leak.
Product
CLEARLINK SYSTEM Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves, 10 drops/mL, 100-inch (2.5 meters), Product Code 2C8425
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0195-2026·2025-10-22
Filtered solution sets recalled from one lot because IV sets may leak
Baxter is recalling 106,176 CLEARLINK System Continu-Flo solution sets with a 0.2 micron filter from one lot because the IV sets may leak.
Product
CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, 0.2 Micron Filter, two CLEARLINK Luer Activated Valves, Backcheck Valve, 10 drops/mL, 104-inch (2.6 meters), Product Code 2C8571
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0196-2026·2025-10-22
Three valve filtered solution sets recalled because IV sets may leak
Baxter is recalling 8,368 CLEARLINK System Continu-Flo solution sets with three luer activated valves and a 0.2 micron filter from one lot because the IV sets may leak.
Product
CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, 0.2 Micron Filter, three CLEARLINK Luer Activated Valves, Backcheck Valve, 10 drops/mL, 102-inch (2.6 meters), Product Code 2C8593
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0166-2026·2025-10-22
Cardiac Workstation 7000 recalled after pinched power module wire caused short
Philips is recalling 29 Cardiac Workstation 7000 units after environmental stress testing failed because a pinched power module wire inside the housing resulted in a short.
Product
Cardiac Workstation 7000; Model Number: 860441;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0143-2026·2025-10-22
Preconnect pump devices recalled over inflation and deflation performance issues
Boston Scientific is recalling 172 CXR Preconnect devices with TENACIO Pump and InhibiZone because of the potential for inflation or deflation performance issues or difficulties.
Product
CXR Preconnect with TENACIO Pump with InhibiZone; UPNs: (1) UPN: 72404461 (12CM PS IZ), (2) 72404462 (14CM PS IZ), (3) 72404463 (16CM PS IZ), (4) 72404464 (18CM PS IZ), (5) 72404465 (10CM IP IZ), (6) 72404466 (12CM IP IZ), (7) 72404467 (14CM IP IZ), (8) 72404468 (16CM IP IZ), (9
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0201-2026·2025-10-22
Non-DEHP Continu-Flo sets recalled from one lot because sets may leak
Baxter is recalling 48,096 CLEARLINK System non-DEHP Continu-Flo solution sets from one lot because the IV sets may leak.
Product
CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves. 10 drops/mL, 96-inch (2.4 meters). Non-DEHP, Product Code 2R8519
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0137-2026·2025-10-22
Anesthesia sets recalled because they contain recalled leaking Clearlink IV sets
Medline is recalling 950 Adult Anesthesia Sets because specific lots may contain Clearlink IV sets that Baxter recalled following customer reports of leaking.
Product
Medline Adult Anesthesia Set, REF DYNJ39985G
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0169-2026·2025-10-22
Monitor display cables recalled over inadequate shielding and electromagnetic interference
Spacelabs Healthcare is recalling 16,898 DVI display cables because inadequate shielding may allow electromagnetic interference with other electronically sensitive medical devices in use.
Product
Brand Name: Branding is not applied to this product. Product Name: DVI display cables Model/Catalog Number: 012-0893-01 Software Version: N/A Product Description: 16 inch DVI-I to DVI-I male/male display cable. Component: Yes, the cable is an external display cable used with
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0131-2026·2025-10-22
Carotid stent systems recalled because integrated filter may not fully open
Contego Medical is recalling 568 Neuroguard IEP carotid stent systems because the integrated filter may not open, or may not fully open, during sheath retraction and filter knob operation.
Product
Neuroguard IEP 3 in 1 Carotid Stent and Post-Dilation Balloon System with Integrated Embolic Protection (Neuroguard IEP System), REF: NG-0740-140-2, NG-NV-7-40, NG-0640-140-2, NG-NV-6-40
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0189-2026·2025-10-22
Stopcock extension solution sets recalled from two lots because sets may leak
Baxter is recalling 49,200 Continu-Flo solution sets with a 4-way stopcock extension set because the IV sets may leak.
Product
CONTINU-FLO Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves, Backcheck Valve, Plus 4-Way Stopcock Extension Set with two CLEARLINK Luer Activated Valve, Pfoduct code 2C6255
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0022-2026·2025-10-22
Sunscreen lotion recalled after failing total aerobic microbial count testing
SV Labs Prescott is recalling 11,386 tubes of Aloe Up Sport Performance Sunscreen Lotion SPF 30 after the firm released and distributed product that failed total aerobic microbial count testing.
Product
Aloe Up Sport Performance Sunscreen Lotion SPF 30, 1 FL OZ (30 mL) per tube, Mfd. for: ALOE UP, 9700 W. 76th St., Ste 112, Eden Prairie, Minnesota 55344
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0168-2026·2025-10-22
Twelve foot display cables recalled over inadequate shielding and interference
Spacelabs Healthcare is recalling 820 twelve-foot DVI display cables because inadequate shielding may allow electromagnetic interference with other electronically sensitive medical devices in use.
Product
Brand Name: Branding is not applied to this product. Product Name: DVI display cables Model/Catalog Number: 012-0895-12 Software Version: N/A Product Description: 12 foot DVI-I to DVI-I male/male display cable. Component: Yes, the cable is an external display cable used with
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0135-2026·2025-10-22
Goniotomy instruments recalled over compromised sterile packaging integrity
Iantrek is recalling 198 C-Rex UNO Microinterventional Goniotomy Instruments over the potential for compromised integrity of the sterile packaging.
Product
C-Rex UNO Microinterventional Goniotomy Instrument. Model Number: CRX-120. Product Description: The C-Rex UNO Microinterventional Goniotomy Instrument is a sterile single use disposable manual surgical instrument used in ophthalmic procedures for ab interno goniotomy and inne
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0177-2026·2025-10-22
Central line insertion kits recalled after being sterilized more than once
American Contract Systems is recalling 32,433 adult central line insertion supply kits that were re-gassed after a nonconformance, without validation for multiple sterilization cycles.
Product
Medical convenience kits Item Number/Description UICL44P ADULT CENTRAL LINE INSERTION SUPPLY KIT UICL44R ADULT CENTRAL LINE INSERTION SUPPLY KIT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0142-2026·2025-10-22
CX preconnect pumps recalled over inflation and deflation performance issues
Boston Scientific is recalling 2,288 CX Preconnect devices with TENACIO Pump and InhibiZone because of the potential for inflation or deflation performance issues or difficulties.
Product
CX Preconnect with TENACIO Pump with InhibiZone; UPNs: (1) UPN: 72404430 (12CM PS IZ), (2) 72404431 (15CM PS IZ), (3) 72404432 (18CM PS IZ), (4) 72404433 (21CM PS IZ), (5) 72404434 (24CM PS IZ), (6) 72404435 (12CM IP IZ), (7) 72404436 (15CM IP IZ), (8) 72404437 (18CM IP IZ), (9)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0145-2026·2025-10-22
Shoulder surgical planning software recalled over possible implant malalignment risk
Kico Knee Innovation Company is recalling 21 ARVIS Shoulder systems after a complaint identified an issue with the AI surgical planning software that may cause implant malalignment.
Product
Brand Name: ARVIS Product Name: ARVIS" Shoulder Model/Catalog Number: IN-27300, Arvis Surgical Planning Software Software Version: V2025.1.2 Product Description: Intended Use: The ARVIS" system is a computer-controlled navigation system intended to provide intra-operative mea
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0187-2026·2025-10-22
Dilation and curettage packs recalled after being sterilized more than once
American Contract Systems is recalling D and C convenience packs that were re-gassed after a sterilization nonconformance, without validation for multiple cycles.
Product
Medical convenience kits IHDC30R D AND C PACK
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0197-2026·2025-10-22
Forty four inch extension sets recalled because the IV sets may leak
Baxter is recalling 15,552 CLEARLINK System 44-inch straight-type extension sets from one lot because the IV sets may leak.
Product
CLEARLINK SYSTEM EXTENSION SET, Straight-Type Extension Set, Standard Bore, CLEARLINK Luer Activated Valve, Retractable Collar, 44-inch (111 centimeters), Product code 2C8610
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0175-2026·2025-10-22
Cardiac catheterization packs recalled after being sterilized more than once
American Contract Systems is recalling cardiac catheterization and cath lab convenience packs that were re-gassed after a sterilization nonconformance.
Product
Medical convenience kits Item Number/Description EVLH67F LEFT HEART CATH PACK FDCL22R CATH LAB ANGIO IHCC03X CATH CARDIAC PACK TNCC02AD CARDIAC CATH TRINITY UICC27AG CARDIAC CATH ANGIO PACK (PS 923077) UIRD89AH RADIAL PACK (PS 56573)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0200-2026·2025-10-22
Filtered extension sets recalled across two lots because IV sets may leak
Baxter is recalling 69,936 CLEARLINK System non-DEHP extension sets with a 1.2 micron filter across two lots because the IV sets may leak.
Product
CLEARLINK System Non_DEHP Extenstion Set, Straight-Type Extension Set, Standard Bore, 1.2 Micron Filter, CLEARLINK Luer Activated Valve, 19-inch (47 centimeters), Product Code 2H8603
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0170-2026·2025-10-22
Basic biopsy trays recalled after entire lot was sterilized more than once
American Contract Systems is recalling a Basic Biopsy Tray lot that was re-gassed after a sterilization nonconformance, without validation for multiple cycles.
Product
Basic Biopsy Tray, Item Number NMBP44L
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0156-2026·2025-10-22
LOGIQ P10 HD systems recalled over inaccurate liver steatosis measurement values
GE is recalling 31 LOGIQ P10 R4.5 HD ultrasound systems running software R4.5.7 because the Ultrasound-Guided Attenuation Parameter measurement may display inaccurate liver steatosis values.
Product
LOGIQ P10 R4.5 HD ultrasound system with system software version R4.5.7., Model Number 5877535
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0178-2026·2025-10-22
Head and neck procedure packs recalled after being sterilized more than once
American Contract Systems is recalling ENT and head and neck convenience packs that were re-gassed after a sterilization nonconformance, without validation for multiple cycles.
Product
Medical convenience kits Item Number/Description RCEN25B ENT SDSC 0246972 RCHN27D HEAD AND NECK RCH 0246951
Category
Medical Device
Distribution
Distributed nationwide