2018 Recalls
7,795 recalls · Page 53 of 156
2018 Recall Year Insight
Federal agencies issued 7,795 product recalls indexed by PlainRecalls in calendar year 2018. That represents about 7.66% of the 101,704 total recalls we track from 1995 through the present, and averages roughly 21.4 recalls per day across the FDA, CPSC, and NHTSA combined. Year-level views are the cleanest way to see macro patterns: volume spikes often correlate with new regulatory priorities (e.g., infant-sleep products after 2021, lithium-ion batteries after 2022), supply-chain contamination events, or changes in agency enforcement intensity, while quiet years can reflect either genuine product-safety improvements or reduced agency staffing and reporting lag. With 156 pages at 50 recalls each, browsing this year end-to-end gives a statistically representative sample of what the federal recall pipeline looked like in 2018.
On this page of 50 records, severity classification shows 4 critical, 45 moderate, and 1 lower-severity recalls. The page references 28 distinct recalling firms operating in 5 distinct product categories, with 34 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (42), CPSC (5), NHTSA (3), which matters because each agency's recall authority, hazard framing, and remedy mechanism differ, an FDA food recall, a CPSC consumer-product recall, and a NHTSA vehicle recall are legally distinct instruments even when the underlying hazard language sounds similar. Reviewing the dominant agency for a given year is one of the fastest ways to understand where federal attention was concentrated.
Year-indexed browsing serves three practical purposes: historical research (tracking how a hazard class evolved over time), consumer action (finding whether a product purchased in 2018 was later recalled), and journalistic or regulatory context (understanding what the enforcement landscape looked like in a given period). Every record on this page links to a full detail view with the hazard, remedy, distribution, and agency-assigned recall number, always use that recall number to verify current status directly with the issuing agency before acting on time-sensitive remedies, because agencies amend, terminate, and expand recalls in the months and years after initial publication. Data on this page reflects federal agency public filings; the agency's live record remains authoritative for legal, medical, or safety decisions. Verify with FDA openFDA, CPSC, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.
Pediatric Two-Lumen Central Venous Catheterization Kit with Blue FlexTip ARROWg+ard Blue Catheter, Cat. No. AK-22502 Product Usage: The multip…
Arrow International Inc
Vertebral Motion Analyzer (VMA), 2.3.239 - 2.3.254. Product Usage: VMA software is a quantitative imaging software application intended to be use…
Ortho Kinematics, Inc
Hitachi Scenaria CT system Product Usage: The SCENARIA CT system is indicated for head, whole body, cardiac and vascular X-ray Computed Tomograph…
Hitachi Medical Systems America Inc
DigitalDiagnost, Single-Detect (Stitching Patient Support) 712062
Philips Medical Systems Gmbh, DMC
DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712082
Philips Medical Systems Gmbh, DMC
BD BBL GC-Lect Agar; Cat. No. 297715 The device is a selective medium providing enhanced growth and recovery of Neisseria gonorrhoeae and better …
Becton Dickinson & Co.
Vertebral Motion Analyzer (VMA), 2.3.250. Product System, image processing, radiological
Ortho Kinematics, Inc
DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026
Philips Medical Systems Gmbh, DMC
3D TOP Ceiling Stand, model no. 3070039 3074486 3070013 3070021 Product Usage: The ceiling stand is used to hold the X-ray tube and / or the d…
Siemens Medical Solutions USA, Inc
GE Healthcare Optima CT660. Sold under the following product names: BEIJING OPTIMA CT660 PRO GT170, BEIJING OPTIMA CT660 PRO GT200, BEIJING O…
GE Healthcare Japan Corporation
Handicare C Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.
Handicare Usa Inc
DigitalDiagnost 4 Chest / Emergency (Stitching Patient Support) 712029
Philips Medical Systems Gmbh, DMC
O-Two Equinox¿ Relieve N2O/O2 Analgesic Gas Mixing and Delivery System Model#: 01EQ1000
O-Two Medical Technologies, Inc.
Philips SureSigns VS2 monitor, 863079 863080 863081 863082 863283 863286 The Sure Signs VS2 vital signs monitor is for use by healthcare pro…
Philips Electronics North America Corporation
EasyDiagnost Eleva DRF, Release 5 (Stitching Patient Support) 706050
Philips Medical Systems Gmbh, DMC
Vertebral Motion Analyzer (VMA), VMA DataLink Software.2.3.231, 2.3.232. Product Usage: VMA software is a quantitative imaging software applicat…
Ortho Kinematics, Inc
Liebel-Flarsheim Direct Digital Imaging System (DDIS) Liebel-Flarsheim urology systems facilitate radiologic and/or fluoroscopic procedures requi…
LIEBEL-FLARSHEIM COMPANY LLC
DigitalDiagnost 4.1 (Stitching Patient Support) 712225
Philips Medical Systems Gmbh, DMC
DigitalDiagnost Classic 1.x Upgrades (Stitching Patient Support) 712081
Philips Medical Systems Gmbh, DMC
MOSAIQ Oncology Information System
Elekta, Inc.
CoLink(TM) Lapidus Plate XP, +2 mm, Right, REF P40 ST165, QTY 1, In2Bones Product Usage: The In2Bones USA LLC, CoLink¿ Plating System is indicat…
In2bones USA, LLC
CombiDiagnost R90 (Stitching Patient Support) 709030
Philips Medical Systems Gmbh, DMC
Handicare P600 Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.
Handicare Usa Inc
DigitalDiagnost Classic, Dual-Detector (Stitching Patient Support) 712052
Philips Medical Systems Gmbh, DMC
Philips SureSigns VS3 Vital Signs Monitor, 863069 863070 863071 863072 863073 863074 The SureSigns VS3 monitor is for monitoring, recording a…
Philips Electronics North America Corporation
Stryker T2 ANKLE ARTHRODESIS NAIL RIGHT 10MMX200MM Item Number: 1819-1020S T2 ANKLE ARTHRODESIS NAIL RIGHT 12MMX200MM 1819-1220S T2 LONG PROXIMAL H…
Stryker GmbH
DigitalDiagnost Dual Detector (Stitching Patient Support) 712022
Philips Medical Systems Gmbh, DMC
CoLink(TM) Lapidus Plate XP, +2 mm, Left, REF P40 ST265, QTY 1, In2Bones Product Usage: The In2Bones USA LLC, CoLink¿ Plating System is indicate…
In2bones USA, LLC
DigitalDiagnost 4 Flex / Value (Stitching Patient Support) 712028
Philips Medical Systems Gmbh, DMC
Artholine Punch B 4, 6MM H 1, 6MM, used for the removal of soft tissue, cartilage tissue or other non-osseous tissue via natural or surgically creat…
Richard Wolf GmbH
GE Healthcare Revolution EVO, Optima CT660, Optima CT670, Optima CT680. The systems are intended for head, whole body, cardiac and vascular X-ray Co…
GE Healthcare Japan Corporation
Vertebral Motion Analyzer (VMA) Version 2.3.252. VMA software is a quantitative imaging software application intended to be used to process digit…
Ortho Kinematics, Inc
DigitalDiagnost, Dual-Detector (Stitching Patient Support) 712052
Philips Medical Systems Gmbh, DMC
is a quantitative/qualitative enzyme-linked immunosorbent assay (ELISA) for the detection of IgG and IgM autoantibodies specific for the phospholipid…
Euro Diagnostica AB
Connecting Bolt, Model 14-442093
Zimmer Biomet, Inc.
bioM¿rieux VITEK 2 NH ID Test Kit Product Usage: Is an automated system consisting of instruments, software and reagent cards designed for the ID…
Biomerieux Inc
Liebel-Flarsheim Hydra Vision Urology X-Ray System (DR) Liebel-Flarsheim urology systems facilitate radiologic and/or fluoroscopic procedures re…
LIEBEL-FLARSHEIM COMPANY LLC
The Tri-Flo Subglottic Suction System
Vyaire Medical
DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031
Philips Medical Systems Gmbh, DMC
GE Healthcare Optima CT540. The systems are intended for head, whole body, cardiac and vascular X-ray Computed Tomography applications.Sold under th…
GE Healthcare Japan Corporation
DigitalDiagnost Rel.4 Upgrades (Stitching Patient Support) 712084
Philips Medical Systems Gmbh, DMC
CAREstream ProNox Nitrous Oxide Delivery System labeled as the following: a. CMI-0100 PNX, Pro-Nox Mixer - Canadian; b. CMI-0100-PNX-HS, Pro…
CAREstream Medical LLC
BSN SPORTS Recalls Rubber Critter Toys Due to Violation of Federal Lead Paint Ban (Recall Alert)
BSN SPORTS LLC, of Farmers Branch, Texas
Cybex Recalls Weight-Lifting Equipment Due to Serious Injury Hazards
Cybex International Inc., of Owatonna, Minn.
TOYOTA 2012: AIR BAGS
TOYOTA
Polaris Recalls RZR XP Turbo S Recreational Off-Highway Vehicles Due to Injury Hazard (Recall Alert)
Polaris Industries Inc., of Medina, Minn
American Landmaster Recalls Off-Road Utility Vehicles Due to Fire and Burn Hazards
ASW, LLC d/b/a American Landmaster, of Columbia City, Ind.
Manhattan Toy Recalls Toy Planes Due to Choking Hazard
The Manhattan Toy Company LLC, of Minneapolis, Minn.
MINI 2017-2019: FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP
MINI
RAM 2018-2019: POWER TRAIN:AXLE ASSEMBLY
RAM
Nearby Recall Years
Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.
Data Sources
- Source: FDA openFDA Enforcement API - calendar-year recall filings for food, drugs, and devices
- Source: CPSC + NHTSA - consumer product and vehicle recall feeds for 2018
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Figures cover calendar year 2018 across the FDA, CPSC and NHTSA federal recall feeds. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.