2019 Recalls
7,396 recalls · Page 78 of 148
2019 Recall Year Insight
Federal agencies issued 7,396 product recalls indexed by PlainRecalls in calendar year 2019. That represents about 8.81% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 20.3 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 148 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 2019.
On this page of 50 records, severity classification shows 16 critical, 30 moderate, and 4 lower-severity recalls. The page references 31 distinct recalling firms operating in 6 distinct product categories, with 42 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (35), NHTSA (8), CPSC (4), 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 2019 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.
Ultra-Drive Irrigation Tubing Assembly, Reference Number 423834 - Product Usage: Item used with the UltraDrive System to provide proper irrigation du…
Zimmer Biomet, Inc.
Kaluza C Flow Cytometry Software, RX Only in the U.S.A., Beckman Coulter, Inc. for the following software devices: (A) Kaluza C Perpetual License…
Beckman Coulter Inc.
Comprehensive Reverse Shoulder Instrument Case Total (Outer Case Vault Only), Item Number 595510
Zimmer Biomet, Inc.
The Tina-quant lgA Gen.2 is an immunoturbidimetric assay. Anti-lgA antibodies react with antigen in the sample to form an antigen/antibody complex wh…
Roche Diagnostics Corporation
Alpha Conducting solution product codes: 3310-25 ASCR - Product Usage: Electrode Conductivity Spray Solution.
Pharmaceutical Innovations, Inc.
A-CIFT SoloFuse Fixed Angle Driver, Model Number 13-32101-01 (Component Part Numbers 14-32107-01 and 14-32106)
SpineFrontier, Inc.
DeRoyal THE RESOURCE GROUP, CRANI PACK, REF 89-9211.07 custom surgical pack
DeRoyal Industries Inc
Aircast REF 3011 - PL RX only VF-PL Sterile Cuff Pkg., Lot# 418003, Expiration Date: 2020 -12 - 31, Made in Mexico, DJO, LLC.
DJO, LLC
Anti-fog solution packaged in a Tyvek peel pouch and it is placed into various kits. Kit are labeled as follows: ROBOTIC GENERAL, LAP CHOLE, GENERA…
Medline Industries, Inc.
Refurbish RIC5-9-D Probe ROHS compliant Ultrasound Probe RIC5-9-D
GE Healthcare, LLC
CS100 Intra-Aortic Balloon Pump, English, 220V; 0998-00-3013-55 For cardiovascular use.
Datascope Corp.
CS100 Intra-Aortic Balloon Pump, English, 110V; 0998-00-3013-53 For cardiovascular use.
Datascope Corp.
CS300 Intra-Aortic Balloon Pump, English, 220V; 0998-00-3023-55 For cardiovascular use.
Datascope Corp.
ElectroMist product codes: 36-3310-60 - Product Usage: Electrode Conductivity Spray Solution.
Pharmaceutical Innovations, Inc.
Advincula Delineator with Ultem Plastic Soft Cup size 3.0 cm; Part No. AD750SC-KE30 The Advincula Delineator Uterine Manipulator is a single-use d…
CooperSurgical, Inc.
Alaris Pump, Model 8100, with bezel mechanical assemblies manufactured with FR-110 plastic resin. The following products are affected by this reca…
CareFusion 303, Inc.
Repair RIC5-9A-RS System, imaging, pulsed doppler, ultrasonic and Refurbish RIC-5-9-D REALTIME 4D
GE Healthcare, LLC
RUSCH Urinary Drainage bag, 2000mlm REF 390060 urine collection device
Teleflex Medical
Erisma- LP posterior fixation system with the below specifically affected products: 1. Erisma-LP polyaxial screws - 4.5, 5.5, 6.5, 7.5, 8.5, 9.5…
Clariance Inc
Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), 0998-00-0800-53 For cardiovascular use.
Datascope Corp.
ElectroMist product codes: 36-3310-04 - Product Usage: Electrode Conductivity Spray Solution.
Pharmaceutical Innovations, Inc.
CS300 Intra-Aortic Balloon Pump, English, 110V; 0998-00-3023-53 For cardiovascular use.
Datascope Corp.
Revolution CT scanners Product Usage: The system is intended for head, whole body, cardiac and vascular X-ray Computed Tomography applications.
GE Healthcare, LLC
Ultra-Drive Hose/Drape Assembly, Reference Number 423833 - Product Usage: Item used with the UltraDrive System to provide proper irrigation during th…
Zimmer Biomet, Inc.
Comprehensive Reverse Shoulder Instrument Case Outer (Outer Case Vault Only), Item Number 595509
Zimmer Biomet, Inc.
Advincula Delineator with Ultem Plastic Soft Cup size 2.5 cm; Part No. AD750SC-KE25 The Advincula Delineator Uterine Manipulator is a single-use d…
CooperSurgical, Inc.
Elekta Unity, Image-Guided Radiation Therapy System Elekta Unity using Magnetic Resonance Imaging is indicated for radiation therapy treatments an…
Elekta, Inc.
Cardiosave Rescue IABP, 0998-00-0800-83 Intra-Aortic Balloon Pump For cardiovascular use.
Datascope Corp.
Teleflex HUDSON RDI NEONATAL ConchaSmart Breathing Circuit with Dual Heated Limb and ConchaSmart Column: a) REF 870-07KIT b) REF 870-09KIT Pro…
Teleflex Medical
TAPSYSTEM Model 2A, REF 8002A
Cardiocommand Inc.
RUSCH CARE Premium Drain bag, 2000mlm REF 390000 urine collection device
Teleflex Medical
Sensation Plus 7.5Fr. 40cc Intra-Aortic Balloon Catheter with accessories, Part Number 0684-00-0568-01 Product Usage: The Sensation Plus 7.5Fr. 4…
Datascope Corporation
Olympus WM-NP2 or WM-DP2 Mobile Workstations with Nurse Control Panel Arm, Model. No. MAJ-1664
Olympus Corporation of the Americas
Alpha Conducting solution product codes:3310-15 ACS - Product Usage: Electrode conductivity spray solution.
Pharmaceutical Innovations, Inc.
BD Microtainer Tube w/ BD Microgard Closure, K2EDTA additive, Model Numbers 365974 and 365975 Product Usage: The Microtainer¿ Brand Tube with EDT…
Becton Dickinson & Company
Porter Cable Table Saws Sold Exclusively at Lowe's Stores Recalled Due to Fire Hazard; Made by Chang Type
Chang Type Industrial Company LTD, of Taichung City, Taiwan
Trek Recalls Kickster Bikes Due to Fall Hazard
Lee Chi Enterprises Co., of Taiwan
FREIGHTLINER 2019-2020: SERVICE BRAKES
FREIGHTLINER
AUDI 2017-2019: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE
AUDI
MERCEDES-BENZ 2019: EQUIPMENT:OTHER:OWNERS/SERVICE/OTHER MANUAL
MERCEDES-BENZ
LEXUS 2019: ELECTRONIC STABILITY CONTROL (ESC)
LEXUS
The Boppy Company Recalls Infant Head and Neck Support Accessories Due to Suffocation Hazard
BMW 2019: WHEELS:LUGS/NUTS/BOLTS/STUDS
BMW
MERCEDES-BENZ 2019-2020: FORWARD COLLISION AVOIDANCE: SENSING SYSTEM: RADAR
MERCEDES-BENZ
KIA 2019: FORWARD COLLISION AVOIDANCE: AUTOMATIC EMERGENCY BRAKING
KIA
GENESIS 2017-2018: ENGINE AND ENGINE COOLING:EXHAUST SYSTEM:MANIFOLD/HEADER/MUFFLER/TAIL PIPE
GENESIS
Factory Direct Wholesale Recalls Folding Mattresses Due to Violation of Federal Mattress Flammability Standard
Relux Mattress Co. LTD, of China
Stagno's Bakery, Inc., P009, Choc Chip Bagel, Case 32lbs. Count per Case 120 of wholesale frozen bagel dough / bulk . Keep Frozen
Stagno's Bakery, Inc.
Gordon CHOICE Whole Strawberries; 5lb bags; UPC Code 93901 24463 5
B.C. Frozen Foods
Stagno's Bakery, Inc., P018, Jalapeno Bagel , Contains Wheat, Soy, Case 32lbs. Count per Case 120 of wholesale frozen bagel dough / bulk . Keep Fro…
Stagno's Bakery, Inc.
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 2019
Read our methodology — how this data is sourced, computed, and verified.