PlainRecalls

2019 Recalls

6,365 recalls · Page 45 of 128

2019 Recall Year Insight

Federal agencies issued 6,365 product recalls indexed by PlainRecalls in calendar year 2019. That represents about 7.58% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 17.4 recalls per day across the FDA, CPSC, NHTSA, and USDA FSIS 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 128 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 2 critical, 48 moderate, and 0 lower-severity recalls. The page references 16 distinct recalling firms operating in 4 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (34), FDA Drug (16), 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, NHTSA, or USDA FSIS for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Drug Moderate Aug 28, 2019

Clear Eyes Assorted IRC Display; each display contains 6 each of a) Clear eyes REDNESS RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.12%) eye d…

Medtech Products, Inc.

FDA Drug Moderate Aug 28, 2019

Clear Eyes Assorted Sidekick Floor Stand Display; each display contains 6 each of a) Clear eyes REDNESS RELIEF (Glycerin 0.25%, Naphazoline hydrochlo…

Medtech Products, Inc.

FDA Drug Moderate Aug 28, 2019

Clear Eyes Maximum Itchy Eye Relief Sidekick Floor Stand Display; each display (case UPC 10678112736383) contains 12 each of Clear eyes MAXIMUM ITCHY…

Medtech Products, Inc.

FDA Drug Moderate Aug 28, 2019

Clear Eyes Redness Relief Handy Pocket Pal Club Pak Display; each display (case UPC 30300742541283) contains 48 each of Clear eyes REDNESS RELIEF (Gl…

Medtech Products, Inc.

FDA Drug Moderate Aug 28, 2019

Clear eyes REDNESS RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.012%) eye drops, Handy Pocket Pal, 0.2 FL OZ (6 mL) bottle, Distributed by Sel…

Medtech Products, Inc.

FDA Drug Moderate Aug 28, 2019

Clear Eyes Redness Relief Club Pack Display; each display contains 18 3-Pack bottles (UPC 6 78112 10552 6) of Clear eyes REDNESS RELIEF (Glycerin 0.2…

Medtech Products, Inc.

FDA Drug Moderate Aug 28, 2019

Clear Eyes Maximum Redness Relief Club Pack Display; each display contains 18 3-Pack bottles (UPC 6 78112 10859 6) of Clear eyes MAXIMUM REDNESS RELI…

Medtech Products, Inc.

FDA Drug Moderate Aug 28, 2019

Clear Eyes Maximum Itchy Eye Relief Sidekick Floor Stand Display; each display contains 12 each of Clear eyes MAXIMUM ITCHY EYE RELIEF (Glycerin 0.25…

Medtech Products, Inc.

FDA Drug Moderate Aug 28, 2019

Bexarotene Capsules, 75 mg, 100 capsules per bottle, Rx Only, Manufactured for: Upsher-Smith Laboratories, LLC, Maple Grove, MN 55369. NDC: 0832-028…

Upsher Smith Laboratories, Inc.

FDA Drug Moderate Aug 28, 2019

Clear eyes REDNESS RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.012%) eye drops, Handy Pocket Pal, 0.2 FL OZ (6 mL) bottle, Dist. by Lil' Drug…

Medtech Products, Inc.

FDA Drug Moderate Aug 28, 2019

Clear eyes REDNESS RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.012%) eye drops, packaged in a) 0.5 FL OZ (15 mL) bottle (UPC 6 78112 25415 6)…

Medtech Products, Inc.

FDA Drug Moderate Aug 28, 2019

Clear eyes MAXIMUM REDNESS RELIEF (Glycerin 0.5%, Naphazoline hydrochloride 0.03%) eye drops, 0.5 FL OZ (15 mL) bottle, Distributed by Medtech Produc…

Medtech Products, Inc.

FDA Drug Moderate Aug 28, 2019

Clear Eyes Redness Relief Hand Pocket Pal Tray Display; each display (UPC 6 78112 25418 7) contains 48 each of Clear eyes REDNESS RELIEF (Glycerin 0.…

Medtech Products, Inc.

FDA Drug Moderate Aug 28, 2019

Clear eyes MAXIMUM ITCHY EYE RELIEF (Glycerin 0.25%, Naphazoline hydrochloride 0.012%, Zinc Sulfate 0.25%) eye drops, 0.5 FL OZ (15 mL) bottle, Distr…

Medtech Products, Inc.

FDA Drug Moderate Aug 28, 2019

Clear Eyes Maximum Redness and Itchy Eye Relief Sidekick Display; each display contains 12 each of a) Clear eyes MAXIMUM REDNESS RELIEF (Glycerin 0.5…

Medtech Products, Inc.

FDA Drug Moderate Aug 28, 2019

Ketamine 50 mg/5 mL in 0.9% Sodium Chloride Injection for IV or IM Use (concentration = 10 mg/mL), 6 mL Syringe, Rx Only, SCA Pharmaceuticals, Windso…

SCA Pharmaceuticals, LLC

FDA Devices Critical Aug 28, 2019

Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Ultra Delivery System) (29mm) 9630TF29 UDI:00690103201260

Edwards Lifesciences, LLC

FDA Devices Moderate Aug 28, 2019

Kit BD Max Enteric Viral Panel RUO; Catalog # 443715

Becton Dickinson & Co.

FDA Devices Moderate Aug 28, 2019

Microdot Xtra blood glucose test strips

Cambridge Sensors Limited

FDA Devices Moderate Aug 28, 2019

Thoratec Heartmate 3 Sealed Outflow Graft with Bend Relief, Sterile, REF 105581US/105581, RX only, Part of Left Ventricular Assist Device (LVAD) U…

Thoratec Corp.

FDA Devices Moderate Aug 28, 2019

BD Vacutainer Lithium HeparinN (LH) 95 USP Units Blood Collection Tubes, Catalog Number 367886

Becton Dickinson & Company

FDA Devices Moderate Aug 28, 2019

BD Vacutainer PST Gel and Lithium HeparinN (LH) 56 Units Blood Collection Tubes, Catalog Number 367960

Becton Dickinson & Company

FDA Devices Moderate Aug 28, 2019

QIAsymphony SP SOW 5.0.3, software used with the QIAsymphony SP Instrument (The QIAsymphony SP instrument is designed to perform automated purificati…

Qiagen Sciences LLC

FDA Devices Moderate Aug 28, 2019

BD Vacutainer PST Gel and Lithium HeparinN (LH) 126 Units Blood Collection Tubes, Catalog Number 367964

Becton Dickinson & Company

FDA Devices Moderate Aug 28, 2019

Kit BD Max StaphSR; Catalog # 443418

Becton Dickinson & Co.

FDA Devices Moderate Aug 28, 2019

BD Vacutainer Lithium HeparinN (LH) 37 USP Units Blood Collection Tubes, Catalog Number 366664

Becton Dickinson & Company

FDA Devices Moderate Aug 28, 2019

Kit BD Max ExK DNA 1 USA; Catalog # 442817

Becton Dickinson & Co.

FDA Devices Moderate Aug 28, 2019

Kit EXT Enteric Bacterial Panel; Catalog # 443812

Becton Dickinson & Co.

FDA Devices Moderate Aug 28, 2019

Kit BD Max Check-Points CPO IVD EU; Catalog # 278102

Becton Dickinson & Co.

FDA Devices Moderate Aug 28, 2019

Brand Name Burn Navigator¿ Model Numbers: Catalog 1120, Burn Navigator¿ H2 Catalog 1125, Burn Navigator¿ H2 Transport Package Burn Navigator Us…

Arcos, Inc

FDA Devices Moderate Aug 28, 2019

BD Vacutainer LH (Lithium Heparin) 34 I.U. Plus Blood Collection Tubes, Catalog Number 368494

Becton Dickinson & Company

FDA Devices Moderate Aug 28, 2019

BD Vacutainer Lithium HeparinN (LH) 56 USP Units Blood Collection Tubes, Catalog Number 366667

Becton Dickinson & Company

FDA Devices Moderate Aug 28, 2019

ACUSON NX2 Elite Diagnostic Ultrasound System, Model # 11284500, RX Only, Siemens Medical Solutions, containing software version VA10A, VA10B, VA11A…

Siemens Medical Solutions USA, Inc.

FDA Devices Moderate Aug 28, 2019

ZYMUTEST HIA MonoStrip, IgG ELISA kit, Model No. RK041A, for in vitro diagnostic use.

Aniara Diagnostica LLC

FDA Devices Moderate Aug 28, 2019

Kit BD Max Enteric Viral Panel EU Catalog # 443985

Becton Dickinson & Co.

FDA Devices Moderate Aug 28, 2019

BD Vacutainer PST Gel and Lithium HeparinN (LH) 56 Units Blood Collection Tubes, Catalog Number 368056

Becton Dickinson & Company

FDA Devices Moderate Aug 28, 2019

MAGNETOM Spectra magnetic resonance diagnostic devices Model # 10837643

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Aug 28, 2019

BD Vacutainer PST Gel and Lithium HeparinN (LH) 83 Units Blood Collection Tubes, Catalog Number 367962

Becton Dickinson & Company

FDA Devices Moderate Aug 28, 2019

Kit BD Max ExK TNA 2; Catalog # 442825

Becton Dickinson & Co.

FDA Devices Critical Aug 28, 2019

Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Ultra Delivery System) (23mm) 9630TF23 UDI:00690103201246

Edwards Lifesciences, LLC

FDA Devices Moderate Aug 28, 2019

Kit BD Max ExK DNA 1 EU LUO; Catalog # 442818

Becton Dickinson & Co.

FDA Devices Moderate Aug 28, 2019

PRO-DEX Surgical Driver Battery Pack PDBP-001 Series PRO-DEX Battery Pack, Single Pouch - PDBP-001-2 PRO-DEX Battery Pack, 40 Pouches - PDBP-040-2 …

Pro-Dex Inc

FDA Devices Moderate Aug 28, 2019

Kit BD Max MRSA; Catalog # 442953

Becton Dickinson & Co.

FDA Devices Moderate Aug 28, 2019

IMMULITE 1000 Progesterone, Model LKPW1, SMN Number 10381128

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Aug 28, 2019

ACUSON NX3 Diagnostic Ultrasound System, Model # 11235612, RX Only, Siemens Medical Solutions, containing software versions: VA10A, VA10B, VA10C, V…

Siemens Medical Solutions USA, Inc.

FDA Devices Moderate Aug 28, 2019

Kit BD Max Vaginal Panel; Catalog # 443712

Becton Dickinson & Co.

FDA Devices Moderate Aug 28, 2019

Kit BD Max ExK DNA 2 EU LUO; Catalog # 442820

Becton Dickinson & Co.

FDA Devices Moderate Aug 28, 2019

Luminex Aries M1 System Model: Aries M6V1 Aries Software v1.0 For In Vitro Diagnostic Use in clinical laboratories. Scanner Label/Labeling…

Luminex Corporation

FDA Devices Moderate Aug 28, 2019

MAGNETOM Prisma magnetic resonance diagnostic devices Model #10849582

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Aug 28, 2019

Kit BD Max StaphSR; Catalog # 443419

Becton Dickinson & Co.

Nearby Recall Years

Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.

Compare 2019 with 2018 →

Data Sources

  • Source: FDA openFDA Enforcement API — calendar-year recall filings for food, drugs, and devices
  • Source: CPSC + NHTSA + USDA FSIS — consumer product, vehicle, and meat/poultry recall feeds for 2019