PlainRecalls

2019 Recall Year Insight

Federal agencies issued 7,611 product recalls indexed by PlainRecalls in calendar year 2019. That represents about 7.29% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 20.9 recalls per day across the FDA, CPSC, USDA FSIS, 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 153 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 3 critical, 47 moderate, and 0 lower-severity recalls. The page references 33 distinct recalling firms operating in 6 distinct product categories, with 47 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (38), FDA Food (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 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, USDA FSIS, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Food Moderate Sep 11, 2019

Vitony Bakery, Bizcocho de Queso y Guayaba (Cheese-Guava Pudding Cake); Peso Neto 14 ONZ. (397 G)

Vitony Bakery, Inc.

FDA Food Moderate Sep 11, 2019

Sweet Basil Farm Hawaii

First Rate Plantation

FDA Food Moderate Sep 11, 2019

Maple Iced Cinnamon Rolls, Net Wt. 1.33 lbs., Walnuts on top in see-through clamshells with clear plastic lids. 8 rolls per clamshell.

Schrock's Sugar 'N Spice LLC

FDA Food Moderate Sep 11, 2019

Nice! Espresso Trail Mix, Net Wt 2.5 Oz (70g) Pouch. Distributed by Sun Tree Snack Foods, LLC, Ambient Storage

Suntree Snack Foods, LLC

FDA Food Moderate Sep 11, 2019

Orange cocktail 3 gallon (384 Fl OZ)

Southern Style Mfg

FDA Devices Moderate Sep 11, 2019

OMNIlife science, Inc. ApeX acetabular liner hip prosthesis component Serf Dual Mobility Cup Insert Liner 51-28; Product code: H6-25128

OMNIlife science Inc.

FDA Devices Moderate Sep 11, 2019

cobas e 601 module (cobas 6000 Modular Series system) Part Number: 04745922001

Roche Diagnostics Operations, Inc.

FDA Devices Moderate Sep 11, 2019

CE17TKFCN EPID TRAY W/ 17GA TUOHY NRFIT Catalog # 339186

B. Braun Medical, Inc.

FDA Devices Moderate Sep 11, 2019

The LeMaitre Aortic Occlusion Catheter is a single lumen catheter with a latex balloon, it is offered in two balloon sizes: 28 mm or 45mm. The single lumen acts as the inflation lumen for the balloon and is indicated by the white stopcock. Other features include a balloon wall thickness designed to reduce the possibility of puncture by calcium deposits, and a stop-cock to maintain balloon inflation level throughout the procedure.

LeMaitre Vascular, Inc.

FDA Devices Moderate Sep 11, 2019

ES1725KFXN ESPOCAN SPINAL/EPID TRY NRFIT Catalog # 339114

B. Braun Medical, Inc.

FDA Devices Moderate Sep 11, 2019

Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel, a component of Berchtold Chromophare Ceiling Mounted Surgical Light System.

Stryker Communications

FDA Devices Moderate Sep 11, 2019

BD Kiestra InoqulA+ Software Version 20.3. IVD automated specimen processing Catalog Number : 447213

Becton Dickinson & Co.

FDA Devices Moderate Sep 11, 2019

HS Hi-R NEO 900A NIR Reference # 657 822 Serial # from 101 Product Usage: A wide range of surgical interventions are made possible through the modular construction and the diversity of the equipment and accessories. The operating microscope HS Hi-R NEO 900/HS Hi-R NEO 900A/HS Hi-R NEO 900A NIR and HS ALLEGRA 900/590/90 are designed for use in Ophthalmology and in other disciplines where a vertical line of viewing is required. Due to their high maneuverability, the HS ALLEGRA range of opera

Haag-Streit USA Inc

FDA Devices Moderate Sep 11, 2019

syngo.CT software version VA48A_SP5.5 in the following SOMATOM computed tomography models: SOMATOM Definition Edge-Model #10590000; SOMATOM Definition AS Model #8098027; SOMATOM Definition Flash Model #10430603

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Sep 11, 2019

DIATECH, swiss dental instruments, ROUND END TAPER, 856-016-7-F

Coltene /Whaledent AG

FDA Devices Moderate Sep 11, 2019

CE17TKFCSN CON EPI TRAY W/17G TUHY NRFIT Catalog # 339187

B. Braun Medical, Inc.

FDA Devices Moderate Sep 11, 2019

HS Hi-R NEO 900 Reference # 657 820 Serial # from 101 Product Usage: A wide range of surgical interventions are made possible through the modular construction and the diversity of the equipment and accessories. The operating microscope HS Hi-R NEO 900/HS Hi-R NEO 900A/HS Hi-R NEO 900A NIR and HS ALLEGRA 900/590/90 are designed for use in Ophthalmology and in other disciplines where a vertical line of viewing is required. Due to their high maneuverability, the HS ALLEGRA range of operating

Haag-Streit USA Inc

FDA Devices Moderate Sep 11, 2019

The Tina-Quant Myoglobin Gen. 2 Tests system is an immuno-turbidimetric assay for the quantitative in vitro determination of myoglobin in human serum and plasma on Roche automated clinical chemistry analyzers

Roche Diagnostics Operations, Inc.

FDA Devices Moderate Sep 11, 2019

CE18TKSTN CONT EPID W/SOFT TIP NRFIT Catalog # 339191

B. Braun Medical, Inc.

FDA Devices Moderate Sep 11, 2019

Titan Gel Serum Protein Control: SPE Control Cat. No 5136 1 x 2.0 mL

Helena Laboratories, Inc.

FDA Devices Moderate Sep 11, 2019

cobas c513 Analyzer

Roche Diagnostics Operations, Inc.

FDA Devices Moderate Sep 11, 2019

Cobas 8000 Modular Analyzer Series: cobas 8000 ISE module part Numbers : 05964075001 cobas c 701 module part Numbers : 05641489001 cobas c 702 module part Numbers : 06473245001

Roche Diagnostics Operations, Inc.

FDA Devices Moderate Sep 11, 2019

SonarMed AirWave Monitor, Model Number M0001

SonarMed Inc

FDA Devices Moderate Sep 11, 2019

CE18TKN ACCU-BLOC PERIFIX KIT NRFIT Catalog # 339188

B. Braun Medical, Inc.

FDA Devices Moderate Sep 11, 2019

CE17TKN CONT EPIDURALTUOHY NRFIT Catalog # 339183

B. Braun Medical, Inc.

FDA Devices Moderate Sep 11, 2019

BD Kiestra InoqulA Software Version 20.3.IVD automated specimen processing Catalog Number: 447202

Becton Dickinson & Co.

FDA Devices Moderate Sep 11, 2019

Alere Cholestech LDX Analyzer, model # 14-874 containing power supplies with the identifying codes of 1837d and 1843d - Product Usage: The Alere Cholestech LDX System is a small, portable analyzer and test cassette system. The System is for in vitro diagnostic use only. The Lipid Profile GLU Cassette is for the quantitative determination of total cholesterol, HDL (high-density lipoprotein) cholesterol, triglycerides and glucose in whole blood. A TC/HDL (total cholesterol/HDL cholesterol) ratio a

Alere San Diego, Inc.

FDA Devices Moderate Sep 11, 2019

HS Hi-R NEO 900A Reference # 657 821 Serial # from 101 Product Usage: A wide range of surgical interventions are made possible through the modular construction and the diversity of the equipment and accessories. The operating microscope HS Hi-R NEO 900/HS Hi-R NEO 900A/HS Hi-R NEO 900A NIR and HS ALLEGRA 900/590/90 are designed for use in Ophthalmology and in other disciplines where a vertical line of viewing is required. Due to their high maneuverability, the HS ALLEGRA range of operating

Haag-Streit USA Inc

FDA Devices Moderate Sep 11, 2019

Integra Jarit GEMINI CLAMP 9 1/4 inch - used in vascular and cardiothoracic procedures used for clamping and occluding vessels. Cat. #140-332

Integra LifeSciences Corp.

FDA Devices Moderate Sep 11, 2019

AMS 800 Artificial Urinary Sphincter AMS 800 Belt Cuff, 4.5 cm Part Number: 72400161

Boston Scientific Corporation

FDA Devices Moderate Sep 11, 2019

Norm-O-Temp model 111Z

Cincinnati Sub-Zero Products LLC, a Gentherm Company

FDA Devices Moderate Sep 11, 2019

Flexible Intubation Fiberscope, Model # 11301AB1

Karl Storz Endoscopy

FDA Devices Moderate Sep 11, 2019

OMNIlife science, Inc. ApeX acetabular liner hip prosthesis component ApeX-LNK crosslinked Acetabular Insert, 10 deg hood; Product Code : H5-54840

OMNIlife science Inc.

FDA Devices Moderate Sep 11, 2019

Fujifilm FDR Go Plus mobile X-ray system

Fujifilm Medical Systems U.S.A., Inc.

FDA Devices Moderate Sep 11, 2019

Norm-O-Temp model 111W

Cincinnati Sub-Zero Products LLC, a Gentherm Company

FDA Devices Moderate Sep 11, 2019

Getinge MCC Flow i Disposable CO2 absorber, used in anesthesia systems.

GETINGE US SALES LLC

FDA Devices Moderate Sep 11, 2019

CE18HKN ACCU-BLOC PERIFIX KIT NRFIT Catalog # 339189

B. Braun Medical, Inc.

FDA Devices Moderate Sep 11, 2019

OMNIlife science, Inc. ApeX acetabular liner hip prosthesis component Serf Dual Mobility Cup Liner 53-28; Product code: H6-25328

OMNIlife science Inc.

FDA Devices Moderate Sep 11, 2019

Alaris EtCO2, Model 8300, UDI: 10885403830013, CareFusion for models 11634567 and 8300ADXeN933

CareFusion 303, Inc.

FDA Devices Moderate Sep 11, 2019

AngioDynamics VenaCure EVLT NeverTouch Procedure Kit, 45CM NEVERTOUCH FRS .018 PROCEDURE KIT PG, Catalog Number 11403012

Angiodynamics, Inc.

FDA Devices Moderate Sep 11, 2019

FEF 100N FLAT EPIDURAL FILTER NRFIT Catalog # 339160

B. Braun Medical, Inc.

FDA Devices Moderate Sep 11, 2019

ES1827KN SPINAL/EPIDURAL TRAY NRFIT Catalog # 339115

B. Braun Medical, Inc.

FDA Devices Moderate Sep 11, 2019

SPECTRALIS with HEYEX2 image management system. a non-contact ophthalmic diagnostic imaging device.

Heidelberg Engineering GmbH

NHTSA No agency class Sep 11, 2019

FORD 2017: SEATS

FORD

CPSC No agency class Sep 10, 2019

Air Rifles Recalled by DIANA Can Unexpectedly Discharge; Risk of Serious Injury and Death

Shaoxing Snowpeak Air Gun Factory, of China

CPSC No agency class Sep 10, 2019

Healing Solutions Recalls Essential Oils Due to Failure to Meet Child Resistant Packaging Requirements; Risk of Poisoning

Healing Solutions LLC, of Phoenix, Ariz.

CPSC No agency class Sep 10, 2019

Ragdoll & Rockets Recalls Children's Loungewear Due to Violation of Federal Flammability Standard

Genexus dba Ragdoll & Rockets, of Gardena, Calif.

USDA FSIS Critical Sep 10, 2019

Hy-Vee Fresh Commissary Recalls Ready-To-Eat Beef and Chicken Products Due to Misbranding and Undeclared Allergens

HY-VEE FRESH COMMISSARY

NHTSA No agency class Sep 6, 2019

CADILLAC,CHEVROLET,GMC 2014-2018: SERVICE BRAKES, HYDRAULIC:POWER ASSIST:VACUUM

CADILLAC,CHEVROLET,GMC

NHTSA No agency class Sep 6, 2019

CHEVROLET,GMC 2019: ELECTRICAL SYSTEM: INSTRUMENT CLUSTER/PANEL

CHEVROLET,GMC

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: USDA FSIS Recalls - calendar-year meat, poultry, and processed egg product recall filings
  • Source: CPSC + NHTSA - consumer product and vehicle recall feeds for 2019

Every figure on PlainRecalls is rendered directly from official FDA, CPSC, USDA FSIS and NHTSA recall records; no number is typed in by an editor. Figures cover calendar year 2019 across the FDA, CPSC, USDA FSIS 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 September 2026.