2018 Recalls
7,795 recalls · Page 71 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 0 critical, 50 moderate, and 0 lower-severity recalls. The page references 20 distinct recalling firms operating in 1 distinct product categories, with 40 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (50), 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.
BioMerieux VIDAS System in combination with Quality Control VIDAS* (QCV*) Product Usage: the Quality Control VIDAS (QCV) is an automated test for…
bioMerieux, Inc.
Ankle Arthrodesis Nail, right T2 Ankle ¿10x300mm, Product Number 18191030S
Stryker GmbH
Femoral Nail, A/R, R1500 T2 Femur ¿12x300 mm, Product Number 18281230S
Stryker GmbH
Percepta CRT-P MRI SureScan, REF W1TR01 Product Usage: The CRT-P models are implantable pulse generators with cardiac resynchronization therapy (…
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Percepta Quad CRT-P MRI SureScan, REF W4TR04 Product Usage: The CRT-P models are implantable pulse generators with cardiac resynchronization ther…
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Innova IGS 630/520/530/540 Interventional Fluoroscopic X-ray Systems
GE Medical Systems, SCS
Discovery IGS 730 Interventional Fluoroscopic X-ray Systems
GE Medical Systems, SCS
Femoral Nail, A/R, R1500 T2 Femur ¿12x360 mm, Product Number 18281236S
Stryker GmbH
Hyalomatrix, Product nos. 651105, 651103, 651104, and 651301 Product Usage: Hyalomatrix is a bi-layered, sterile, flexible, and comfortable wound…
Anika Therapeutics, Inc.
Peripherally Inserted Midline Catheter Kit with Placement Wire, REF MK-02031-TW Product Usage: To provide real time tip location information of a…
Arrow International Inc
Reliance 1227 Cart and Utensil Washer/Disinfector, FW03101, FW03102, FW03S003 Product Usage: The Reliance 1227 Cart and Utensil Washer/Disinfecto…
Steris Corporation
BARD MYPICC Kit, REF CK000095B, 5F French Size, packaged 5 kits/case, Sterile, RX, For use in vascular access procedures.
Medline Industries, Inc.
VPS TipTracker Stylet Accessory, REF RHY-177-TTSAP Product Usage: To provide real time tip location information of a central venous catheter by u…
Arrow International Inc
Femoral Nail, LEFT T2 GTN ¿14x300 mm, Product Number 18501430S
Stryker GmbH
BCI Advisor Vital Signs Monitor, Model 9200, Reorder numbers 920654235, 920654235, 920654335A, and 920674235A. (The differences in the reorder numbe…
Smiths Medical ASD Inc.
Percepta Quad CRT-P MRI SureScan, REF W4TR01 Product Usage: The CRT-P models are implantable pulse generators with cardiac resynchronization ther…
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Femoral Nail, RIGHT T2 GTN ¿14x460 mm, Product Number 18511446S
Stryker GmbH
Cryptococcal Antigen Lateral Flow Assay (CrAg LFA), Model # CR2003 Product Usage: The CrAg Lateral Flow Assay is an immunochromatographic test sys…
Immuno-Mycologics, Inc
da Vinci Xi EndoWrist Stapler 45 Reload Green, Model 48445G-03, 12 reloads/box.
Intuitive Surgical, Inc.
Medtronic EnTrust Dual Chamber Implantable Cardioverter Defibrillator with Atrial and Ventricular Therapies and RapidRead Telemetry, D153ATG Produ…
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
VPS Rhythm ECG Accessory Pack, REF RHY-100-ECGO Product Usage: To provide real time tip location information of a central venous catheter by util…
Arrow International Inc
Ankle Arthrodesis Nail, right T2 Ankle ¿11x300mm, Product Number 18191130S
Stryker GmbH
Medtronic EnTrust Escudo D144DRG (OUS distribution) Product Usage: The implantable cardioverter defibrillator is intended to provide ventricular a…
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Femoral Nail, A/R T2 Femur ¿10x340 mm, Product Number 18251034S
Stryker GmbH
Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with Atrial and Ventricular Therapies and RapidRead Telemetry, D154VRC Prod…
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Femoral Nail, A/R T2 Femur ¿15x240 mm, Product Number 18251524S
Stryker GmbH
Femoral Nail, LEFT T2 GTN ¿10x360 mm, Product Number 18501036S
Stryker GmbH
Femoral Nail, A/R, R1500 T2 Femur ¿10x320 mm, Product Number 18281032S
Stryker GmbH
Femoral Nail, RIGHT T2 GTN ¿9x320 mm, Product Number 18510932S
Stryker GmbH
Coronary Sinus (CS) Uni-Directional Diagnostic Electrophysiology (EP) Catheter, catalog numbers D135303 and D135304. Product Usage: The Reprocess…
Stryker Sustainability Solutions
Medtronic EnTrust Dual Chamber Implantable Cardioverter Defibrillator with Atrial and Ventricular Therapies and RapidRead Telemetry, D154ATG Produ…
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Discovery IGS 740 Interventional Fluoroscopic X-ray Systems
GE Medical Systems, SCS
PD-L1 IHC 22C3 pharmDx is a companion diagnostic used to determine PD-L1 levels for determination of patient treatment options.
Dako North America Inc.
Tibial Nail, Standard T2 Tibia ¿12x315 mm, Product Number 18221231S
Stryker GmbH
BioMerieux mini VIDAS System in combination with Quality Control VIDAS* (QCV*) Product Usage: the Quality Control VIDAS (QCV) is an automated tes…
bioMerieux, Inc.
Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with Atrial and Ventricular Therapies and RapidRead Telemetry, D153VRC Prod…
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Femoral Nail, LEFT T2 GTN ¿12x360 mm, Product Number 18501236S
Stryker GmbH
Femoral Nail, A/R, R1500 T2 Femur ¿12x380 mm, Product Number 18281238S
Stryker GmbH
Proteus 235, Version PTS-11.0.1.2 and PTS-11.0.2 Product Usage: A device designed to produce and deliver a proton beam for the treatment of patie…
Ion Beam Applications S.A.
LigaSure" Exact Dissector Nano Coated 20.6mm-21cm Product Usage: A bipolar electrosurgical instrument intended for use in open surgical procedure…
Covidien LLC
NOVAPLUS(R) Pregnancy Cassette Device with Droppers, Urine hCG Pregnancy Cassette, Cat. No. VPT1-CASS Product Usage: pregnancy test
Ekla Corporation
Percepta CRT-P MRI SureScan, REF W1TR04 Product Usage: The CRT-P models are implantable pulse generators with cardiac resynchronization therapy (…
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medtronic EnTrust Escudo D144VRC (OUS distribution) Product Usage: The implantable cardioverter defibrillator is intended to provide ventricular a…
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Femoral Nail, A/R T2 Femur ¿12x360 mm, Product Number 18251236S
Stryker GmbH
Vacuum Regulator, Push-T-Set Intermittent Suction Unit (PTS-ISU) Product Usage: The vacuum regulator is intended to be used in a medical facilit…
Ohio Medical Corporation
Elecsys Vitamin D total II, Vitamin D Test System, Material number 07464215160 Product Usage: This assay is intended for the quantitative determi…
Roche Diagnostics Corporation
da Vinci Xi EndoWrist Stapler 45 Reload Blue, Model 48645B-03, 12 reloads/box.
Intuitive Surgical, Inc.
Elecsys Vitamin D total II, Vitamin D Test System, Material number 07028148190 Product Usage: This assay is intended for the quantitative determi…
Roche Diagnostics Corporation
AperFix AM Femoral Implant, Model numbers CM-2409 (9mm x 24 mm) and CM-2410 (10 mm x 24 mm). For orthopedic use in ligament reconstruction.
Cayenne Medical Inc.
FDI FORT DEFIANCE INDUSTRIES P2131 AUTOMATED FIELD STEAM STERILIZER, NSN: 6530-01-641-4641 Product Usage: The Fort Defiance Industries Automated …
Fort Defiance Industries, LLC
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 August 2026.