PlainRecalls

2019 Recalls

7,396 recalls · Page 115 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 3 critical, 44 moderate, and 3 lower-severity recalls. The page references 27 distinct recalling firms operating in 6 distinct product categories, with 49 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (34), FDA Drug (9), FDA Food (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.

FDA Food Moderate Apr 3, 2019

Vanilla Pound Cake, brand Surtidoras Bakery, net wt. 15 oz., packaged in flexible plastic film wrap. No UPC. The allergens declared in the INGREDI…

Surtidoras Bakery Inc

FDA Food Critical Apr 3, 2019

Soom Chocolate Sweet Tahini Halva Spread 30 ml ( 1oz )Squeeze Pack

Soom Foods

FDA Food Moderate Apr 3, 2019

QVC 3/8 oz bags for Christmas

Bauer's Candies, Inc.

FDA Food Moderate Apr 3, 2019

1 lb salted combo modjeskas

Bauer's Candies, Inc.

FDA Drug Moderate Apr 3, 2019

Express Gel Hand Sanitizer (Ethyl Alcohol 70%), 37 mL (1.25 fl oz) bottles, Ecolab, 370 Wabasha Street N, St. Paul, MN 55102. NDC 47593-502-49

Ecolab Inc

FDA Drug Moderate Apr 3, 2019

Moisturizing Gel Hand Sanitizer (Ethyl Alcohol 62%), 118 mL (4 fl oz) bottles, Ecolab, 370 Wabasha Street N, St. Paul, MN 55102. NDC 47593-489-33

Ecolab Inc

FDA Drug Moderate Apr 3, 2019

Advanced Gel Hand Sanitizer (Ethyl alcohol 62%), packaged in a) 37 mL (1.25 fl oz) bottles (NDC 47593-488-49) and b) 540 mL (18 fl oz) bottles (NDC 4…

Ecolab Inc

FDA Drug Moderate Apr 3, 2019

Fayosim (levonorgestrel and ethinyl estradiol) tablets USP, (0.15 mg/0.02 mg, 0.15 mg/0.025 mg, 0.15 mg/0.03 mg) and ethinyl estradiol tablets USP, (…

Lupin Pharmaceuticals Inc.

FDA Drug Moderate Apr 3, 2019

Quick-Care Foam Hand Sanitizer (Ethyl alcohol 62%), 45 mL (1.5 fl oz) bottles, Ecolab, 370 Wabasha Street N, St. Paul, MN 55102. NDC 47593-491-85

Ecolab Inc

FDA Drug Critical Apr 3, 2019

Blue Fusion Capsules, 1- count blister pack, Distributed by: DNS Distribution 5225 Canyon Crest Dr. Ste 71-640, Riverside, CA 92507, UPC 7 48252 6646…

Ata International Inc

FDA Drug Low Apr 3, 2019

Diclofenac Sodium Topical Solution, 1.5% w/w, 5 FL. OZ. (150 mL) bottle, Rx Only, Manufactured for: Ingenus Pharmaceuticals, LLC, Orlando, FL 32839-…

Ingenus Pharmaceuticals Llc

FDA Drug Moderate Apr 3, 2019

Combigan (brimonidine tartrate/timolol maleate ophthalmic solution) 0.2%/0.5% 5 mL bottles, Rx only, Allergan, Inc. Irvine, CA 92612 U.S.A. NDC 0023…

Allergan Sales, LLC

FDA Drug Moderate Apr 3, 2019

Gel Hand Sanitizer (Ethyl Alcohol 70%), packaged in a) 37 mL (1.25 fl oz) bottles (NDC 47593-487-49), b) 118 mL (4 fl oz) bottles (NDC 47593-487-33…

Ecolab Inc

FDA Devices Moderate Apr 3, 2019

Paltop Premium Surgical Kit-containing the 1.25mm Hex Driver For surgical and restorative applications prosthetic devices, such as artificial teeth …

Keystone Dental Inc

FDA Devices Moderate Apr 3, 2019

LW Scientific ZIP IQ PCV Centrifuge, ZIC-24HD-75T3 Rev C Product Usage: used as a general purpose centrifuge to spin down blood in hematocrit tub…

LW Scientific, Inc.

FDA Devices Moderate Apr 3, 2019

JOURNEY II XR TIBIAL POSTERIOR KEEL PUNCH SZ 3-4 , REF 74013987 The JOURNEY II XR Tibial Posterior Keel Punch is a reusable surgical instrument us…

Smith & Nephew, Inc.

FDA Devices Low Apr 3, 2019

Medtronic Pulmonary Vein Ablation Catheter(R) GOLD (PVAC GOLD) 990078 - Product Usage: The Pulmonary Vein Ablation Catheter GOLD is designed to be us…

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

FDA Devices Moderate Apr 3, 2019

Sunset Compressor Nebulizer, Model NEB100 - Product Usage: The Sunset Compressor Nebulizer is an AC-powered air nebulizer compressor system intended …

SANRAI INTERNATIONAL LLC

FDA Devices Moderate Apr 3, 2019

MultiDiagnost-Eleva, Product codes 708032, 708036 Product Usage: As a multifunctional I universal imaging application system, General RIF, Fluoro…

Philips North America, LLC

FDA Devices Moderate Apr 3, 2019

Omnidiagnost Classic, Product Codes 70859, 708023, 708024, 708025 Product Usage: The Philips OmniDiagnost is a multi-functional, universal X-ray …

Philips North America, LLC

FDA Devices Moderate Apr 3, 2019

JOURNEY II XR TIBIAL POSTERIOR KEEL PUNCH SZ 7-8 , REF 74013988 The JOURNEY II XR Tibial Posterior Keel Punch is a reusable surgical instrument us…

Smith & Nephew, Inc.

FDA Devices Moderate Apr 3, 2019

ICU Medical, Transpac IV Monitoring Kit With Safeset Reservoir and Blood Sampling Port, 152 cm (60") Tubing, Disposable Transducer, 03 ml Squeeze Flu…

ICU Medical, Inc.

FDA Devices Moderate Apr 3, 2019

Paltop Fully Guided Surgical Kit- containing the 1.25mm Hex Driver For surgical and restorative applications prosthetic devices, such as artificial …

Keystone Dental Inc

FDA Devices Moderate Apr 3, 2019

ICU Medical, Transpac IV Monitoring Kit With Safeset Reservoir and Blood Sampling Port, 60" Tubing, Disposable Transducer, 3 ml Intraflo Flush, Macro…

ICU Medical, Inc.

FDA Devices Low Apr 3, 2019

Integrated ECG cable with 3-lead leadwires labeled as the following: 1. ECG TRUNK CABLE, 3-LD W/ INTEGRATED GRABBER LEAD WIRE, AHA, 3.6 M/12 FT…

GE Healthcare, LLC

FDA Devices Moderate Apr 3, 2019

LW Scientific ZIP IQ Combo Centrifuge, ZIC-CMBO-4RT3 Rev B Product Usage: used as a general purpose centrifuge to spin down blood in hematocrit t…

LW Scientific, Inc.

FDA Devices Moderate Apr 3, 2019

Kendall SCD Express Sterile Sleeves (Thigh Length), Model Number 9736

COVIDIEN LLC

FDA Devices Moderate Apr 3, 2019

MultiDiagnost Eleva w/ Flat Detector, Product codes 708034, 708037, 708038 Product Usage: As a multifunctional I universal imaging application sys…

Philips North America, LLC

FDA Devices Moderate Apr 3, 2019

URODiagnost Eleva, Product codes 708026, 708027, 708028 Product Usage: The Philips OmniDiagnost is a multi-functional, universal X-ray system wit…

Philips North America, LLC

FDA Devices Moderate Apr 3, 2019

Vacuum Unit for CATSmart Vacuum Pump. Fresenius CATSmart (Continuous Autotransfusion System) is indicated for the processing of blood collected in…

Fenwal Inc

FDA Devices Moderate Apr 3, 2019

Laparotomy Sponge with the following product description and model numbers: 1. Lap 18X18 XR (5 each/pack, 20 pack/case) - Model Number 300, 450…

Medical Action Industries Inc

FDA Devices Critical Apr 3, 2019

Cardiohelp Emergency Drive, Part No. 70104.8002 Product Usage: The Cardiohelp Emergency Drive is used in emergencies to manually drive the dispos…

Maquet Cardiovascular Us Sales, Llc

FDA Devices Moderate Apr 3, 2019

JOURNEY II XR TIBIAL POSTERIOR KEEL PUNCH SZ 5-6 , REF 74013988 The JOURNEY II XR Tibial Posterior Keel Punch is a reusable surgical instrument us…

Smith & Nephew, Inc.

FDA Devices Moderate Apr 3, 2019

ICU Medical, Transpac IV Monitoring Kit With Safeset Reservoir and Blood Sampling Port, 60" Tubing, Disposable Transducer, 3 ml Squeeze Flush, Macrod…

ICU Medical, Inc.

FDA Devices Moderate Apr 3, 2019

LW Scientific ZIP IQ Combo Centrifuge, ZIC-CMBO-2RT3 Rev B Product Usage: used as a general purpose centrifuge to spin down blood in hematocrit t…

LW Scientific, Inc.

FDA Devices Moderate Apr 3, 2019

Randox Blood Gas Control Level 2 -Model BG5002. In-vitro Diagnostic Quality control of Blood Gas analysis This product is intended for in vitro d…

Randox Laboratories Ltd.

FDA Devices Moderate Apr 3, 2019

BVI Visitec Soft Tip Cannula, 0.8MM .50 x 33mm (25G x 1.3 in). The BVI Soft Tip Cannula is intended to irrigate and/or aspirate ophthalmic solutio…

Beaver Visitec

FDA Devices Moderate Apr 3, 2019

On-X Aortic Heart Valve with Anatomic Sewing Ring Product Usage: The On-X Prosthetic Heart Valve is indicated for the replacement of diseased, da…

CryoLife, Inc.

FDA Devices Moderate Apr 3, 2019

Lithium-ion Rechargeable Batteries for the Philips MX40 Wearable Monitor REF: 989803176201 - Product Usage: Indicated for use by health care professi…

Philips North America, LLC

FDA Devices Moderate Apr 3, 2019

BD Synapsys Laboratory Solutions Catalog Number:444150 Product Usage: BD Synapsys is a laboratory software solution providing data management a…

Becton Dickinson & Co.

FDA Devices Moderate Apr 3, 2019

Avitus¿ Bone Harvester w/ Filter Insert - 8mm intended to harvest cancellous bone and bone marrow Catalog Number: BH-110 The Avitus¿ Bone Harv…

Avitus Orthopaedics, Inc.

FDA Devices Moderate Apr 3, 2019

Paltop 1.25 Hex Drivers, Short Part Number: 60-70102

Keystone Dental Inc

FDA Devices Moderate Apr 3, 2019

JOURNEY II XR TIBIAL POSTERIOR KEEL PUNCH SZ 1-2 , REF 74013986 The JOURNEY II XR Tibial Posterior Keel Punch is a reusable surgical instrument us…

Smith & Nephew, Inc.

FDA Devices Moderate Apr 3, 2019

Paltop 1.25 Hex Drivers, Long Part Number: 60-70101

Keystone Dental Inc

FDA Devices Moderate Apr 3, 2019

Urodiagnost, Product No. 708033 Product Usage: The Philips UroDiagnost MRF can be used to perform all urological and gynecological routine examin…

Philips North America, LLC

FDA Devices Moderate Apr 3, 2019

Accelerate Pheno system, with Accelerate Pheno System Software 1.2.1 - 1.3.1, PSW000012B Product Usage: The Accelerate Pheno system is intended t…

Accelerate Diagnostics Inc

FDA Devices Moderate Apr 3, 2019

Avitus¿ Bone Harvester w/ Filter Insert - 5mm intended to harvest cancellous bone and bone marrow Catalog Number: BH-210 The Avitus¿ Bone Harve…

Avitus Orthopaedics, Inc.

CPSC Moderate Apr 3, 2019

Matco Tools Wireless Chargers Recalled by Professional Tool Products Due to Burn Hazard

CPSC Moderate Apr 3, 2019

Quality Bicycle Products Recalls Bicycles Due To Injury Hazard

NHTSA Moderate Apr 3, 2019

FORD 2014-2017: EQUIPMENT ADAPTIVE/MOBILITY

FORD

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 — consumer product and vehicle recall feeds for 2019