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 8 critical, 40 moderate, and 2 lower-severity recalls. The page references 32 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 (33), FDA Food (11), FDA Drug (6), 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 Oct 30, 2019

Conventional Basil with Basil Infinite Herbs & Specialties brand label. Basil was packed in 2.5 oz plastic clamshell, 4.0 oz. plastic clamshell, and 1 lb plastic bags.

Infinite Herbs, LLC

FDA Food Critical Oct 30, 2019

Ample Hills Peppermint Pattie ice cream packed in 3 gallon tubs and half pint (8oz) cartons . Allergens: Contains: eggs, milk, soy

AMPLE HILLS MANUFACTURING

FDA Food Critical Oct 30, 2019

The Benedict Brunch Bowl; 9.7 oz. UPC: 813377 022854

Urban Remedy

FDA Food Critical Oct 30, 2019

Green Tea Leaf Salad 6.7 oz. UPC: 813377 023158

Urban Remedy

FDA Food Critical Oct 30, 2019

Premo and Fresh Grab Chicken Salad wheat sandwiches, 5 oz., with UPC code 612510002032.

Lipari Foods Operating Company, LLC.

FDA Food Low Oct 30, 2019

NIKKENWELLNESS KENZEN brand Calcium Complex Dietary Supplement 60 Tablets. Label reads "Contains ingredients derived from dairy" under Recommended Use.

HP Ingredients

FDA Food Critical Oct 30, 2019

Jayleaf Fresh Baby Spinach; 4 lb. box (1 x 4 lb. bag) and 12 lb. crate (3 x 4 lb. bags); Refrigerate

Veritable Vegetable

FDA Food Moderate Oct 30, 2019

Trails End Sweet and Savory Collection, containing White Cheddar cheese Corn (5 oz.), Butter Toffee Carmel Corn (20 oz.), and Chocolatey Caramel Crunch (15 oz.) each in individual foil bags packaged together in variety box

weaver fundraising

FDA Food Critical Oct 30, 2019

Premo Signature Cranberry Almond Chicken Salad croissant sandwich, 5 oz., with UPC code 612510090954

Lipari Foods Operating Company, LLC.

FDA Food Critical Oct 30, 2019

Chicken Salad Sandwich, UPC 2 07209-XXXXX. Keep Refrigerated.

Coborn's, Inc

FDA Food Critical Oct 30, 2019

Tuna salad under the following brand names: BALLARDS FARM Barboursville, WV 25504 UPC 076010000293 12 oz. plastic container, LAURA LYNN UPC 086854035368 12 oz. plastic container, MRS. STRATTON S SALADS Birmingham, AL 35219 UPC 075217100294 12 oz. plastic container, STAR FOOD PRODUCTS Burlington, NC 27215 UPC 077541006051 11 oz. plastic container.

Mrs. Stratton's Salads, Inc

FDA Drug Moderate Oct 30, 2019

Amino Acid Injection 50 g/1000 mL (50 mg/mL) 25 g L-Arginine HCl; 25 g L-Lysine HCl, Single Dose Container, Rx Only Nephron 503B outsourcing facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-988-10

Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

FDA Drug Moderate Oct 30, 2019

PF-Fentanyl Citrate 2 mcg/mL* & Bupivacaine HCl 0.125% in 0.9% Sodium Chloride Injection-250 mL, Rx Only Total Dose: (500 mcg/312.5 mg)/250 mL, Nephron 503B Outsourcing Facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-530-25

Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

FDA Drug Moderate Oct 30, 2019

PF-Fentanyl Citrate (2 mcg/mL)* & Bupivacaine HCl 0.0625 in 0.9% Sodium Chloride Injection-250 mL Total Dose: (500 mcg/156.3 mg)/250 mL, Rx Only, Nephron 503B Outsourcing Facility 4500 12th St. Extension West Columbia, SC 29172 NDC 69374-0525-25

Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

FDA Drug Moderate Oct 30, 2019

del Nido Cardioplegia Solution, 1000 mL, Single-Dose Container, Rx Only Nephron 503B Outsourcing Facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-984-10

Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

FDA Drug Moderate Oct 30, 2019

PF-Fentanyl Citrate 2 mcg/mL* & Ropivacaine HCl 0.1% in 0.9% Sodium Chloride Injection-200 mL Total Dose: (400 mcg/200 mg)/200 mL, Rx Only Nephron 503B Outsourcing Facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-526-20

Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

FDA Drug Moderate Oct 30, 2019

Povidone Iodine, 5% Ophthalmic Solution, 5 mL per droptainer, Repackaged by: Avella Specialty Pharmacy, 24416 N. 19th Ave., Phoenix, AZ 85085. NDC 42852-006-20

Avella of Deer Valley, Inc. Store 38

FDA Devices Moderate Oct 30, 2019

Torrent Suite Dx Software Version 5.8 Catalog Number:A36601 and A36602 OEM Customer software: Torrent Suite Dx T430 Software v5.0 DARUI DR-SEQ 800 Software UDI:(01)10190302014090 (11)000000(10)5.8 (240)A36601

Life Technologies Holdings Pte Ltd

FDA Devices Moderate Oct 30, 2019

Canister HFC-134a /1000g, ALUM Product Number: 1600-00-0218 Revision .0C Coolant canister for use with surgical laser.

Candela Corporation

FDA Devices Moderate Oct 30, 2019

Atellica IM 1300 Analyzer, (SW) version V1.19.0 and V1.19.2 Siemens Material Number (SMN): 11066001

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Oct 30, 2019

BD Vacutainer¿ Push Button Blood Collection Set with Pre-Attached Holder Catalog number 368356 - Product Usage: This product is designed to provide customers an increased level of safety during IV blood collection, convenience and to improve OSHA single-use holder compliance. Figure 1 shows a BD Vacutainer¿ Push Button Blood Collection Set with the needle protector removed prior to needle retraction.

Becton Dickinson & Company

FDA Devices Moderate Oct 30, 2019

The ICS CHARTR EP 200

GN Otometrics

FDA Devices Moderate Oct 30, 2019

Canister HFC-134a /1000g, ALUM, 15 pack Product Number: 1600-00-0219 Revision .0C Coolant canister for use with surgical laser.

Candela Corporation

FDA Devices Moderate Oct 30, 2019

Atellica IM 1600 Analyzer, (SW) version V1.19.0 and V1.19.2 Siemens Material Number (SMN): 11066000

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Oct 30, 2019

IMRIS MR/X-ray head fixation device, Model HFD200

Deerfield Imaging, Inc.

FDA Devices Moderate Oct 30, 2019

EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with the following product code and sizes: 1. H938737, 250mL; 2. H938738, 500mL; 3. H938739, 1000mL; 4. H938740, 2000mL; 5. H938741, 3000mL Product Usage: The EXACTAMIX Empty EVA bags are used as the destination container in compounding of large-volume sterile solutions for further administration to a single patient. The empty bags are used at pharmacies and compounding centers by pharmacists and pharmacy technicians to

Baxter Healthcare Corporation

FDA Devices Moderate Oct 30, 2019

Sterile Co-Flex NL 3" - Product Usage: Single Use secondary wound dressing or compression wrap.

Andover Healthcare Inc.

FDA Devices Moderate Oct 30, 2019

GRIPPER Needles sold individually. Labeled as the following item descriptions: 1. NDL, GRIPPER, 22G X 1" (25MM), 12/BX; 2. NDL, GRIPPER, 22G X 1.25" (32MM), 12/BX; 3. NDL, GRIPPER, 20G X 1.25" (32MM), 12/BX; 4. NDL, GRIPPER, 19G X 1" (25MM), 12/BX; 5. NDL, GRIPPER, 19G X 1.25" (32MM), 12/BX; 6. NDL, GRIPPER, 22G X .75" (19MM), 12/BX; 7. NDL, GRIPPER, 19G X .75" (19MM), 12/BX; 8. NDL, GRIPPER, 20G X .625" (16MM), 12/BX; 9. NDL, GRIPPER, 22G X .625" (1

Smiths Medical ASD Inc.

FDA Devices Low Oct 30, 2019

OptiLITE, Products for Laser Surgery, Model # CGH1080F, 800 micron single-use holmium fiber assembly with flat tip, Lot Number 21144, Sterilized by Sterrad Run 4149, This device is for single-use only, sterile, UDI: 00855430006036

Xintec Corp

FDA Devices Moderate Oct 30, 2019

Rifton TRAM Standard Base, SKU K310, powered lift device

Community Products, LLC

FDA Devices Moderate Oct 30, 2019

Sterile Co-Flex LF2 3" - Product Usage: Single Use secondary wound dressing or compression wrap

Andover Healthcare Inc.

FDA Devices Moderate Oct 30, 2019

Patient Data Manager, Model/Catalogue Numbers: 25100-09 - PATIENT DATA MANAGER 2.1.1LICENSE ONLY 25100-10 - PATIENT DATA MANAGER 2.2.0 LICENSE ONLY 25100-11 - PATIENT DATA MANAGER 2.2.1 LICENSE ONLY 25100-12 - PATIENT DATA MANAGER 2.3 INSTALLER 25100-12A - PATIENT DATA MANAGER 2.3.1 INSTALLER 25100-13 - PATIENT DATA MANAGER 2.3 LICENSE 25100-12B - PATIENT DATA MANAGER 2.4.0 INSTALLER 25100-13A - PATIENT DATA MANAGER 2.4 LICENSE 25100-12C - PATIENT DATA MANAGER 2.5.0 INSTALLER

Brainlab AG

FDA Devices Moderate Oct 30, 2019

Torrent Suite Dx Software Version (IUO) 5.2 Catalog Number: A29225 OEM Customer Software: Sentosa SQ Suite Software v5.6.9

Life Technologies Holdings Pte Ltd

FDA Devices Moderate Oct 30, 2019

Mammomat Revelation with software version VC10 and Biopsy Option Intended Use: For mammography exams, screening, diagnostics, biopsies and dual energy procedures

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Oct 30, 2019

Sterile Co-Flex Med 3" - Product Usage: Single Use secondary wound dressing or compression wrap

Andover Healthcare Inc.

FDA Devices Moderate Oct 30, 2019

Rifton TRAM Low Base, SKU K320, powered lift device

Community Products, LLC

FDA Devices Moderate Oct 30, 2019

Semi-Rigid Suction Canister, 3000cc. Model Numbers OR530 and OR530H. For OR530, the product comes in a case with two boxes. One box includes 50 eaches of liners in a poly bag and the second box includes 50 eaches of lids in a poly bag. For OR530H, the customer receives the number of liners and lids purchased in one case without the individual boxes. The "H" denotes a single quantity when being ordered.

Medline Industries Inc

FDA Devices Moderate Oct 30, 2019

GRIPPER Needles sold as part of PORT-A-CATH II SINGLE LUMEN SYSTEM. Labeled as the following item descriptions: 1. TRAY, PAC, VEN, TI, PU, 1.9MM, UL, 6FR/INTRO 1/EA; 2. TRAY, PAC, VEN LP, TI, PU, 1.9MM, UL, 6 FR/INTRO 1/EA; 3. TRAY, PAC II, VEN, 2.8MM, CS, 9FR/INTRO 1/EA; 4. TRAY, PAC II, VEN, TI, PU, 1.9MM, UL, 6FR/INTRO 1/EA; 5. TRAY, PAC II, VEN, PU, 2.6MM, UL, 8.5FR/INTRO 1/EA; 6. TRAY, PAC II, VEN, PU, 2.6MM, PRE-AY, 8.5FR/INTRO 1/EA;

Smiths Medical ASD Inc.

FDA Devices Moderate Oct 30, 2019

Emerald Diluent Tubing, List number 09H50-01, accompanying CELL-DYN Emerald instrument, List number 09H39-01. The firm name on the label is Abbott Laboratories, Abbott Park, IL.

Abbott Laboratories

FDA Devices Moderate Oct 30, 2019

Arrow AGB+ Multi-Lumen CVC Kit-catheter permits venous access to central circulation by way of subclavian, jugular, and femoral veins Product Code: CDC-42703-1A - Product Usage: The ARROWg+ard Blue PLUS catheter permits venous access to central circulation by way of subclavian, jugular, and femoral veins. The ARROWg+ard technology is intended to provide protection against catheter-related bloodstream infections (CRBSIs). It is not intended to be used as a treatment for existing infections nor i

Arrow International Inc

FDA Devices Moderate Oct 30, 2019

Irrisept Wound Debridement and Cleansing System. 12 units per case.

IrriMAX Corporation

FDA Devices Moderate Oct 30, 2019

Sterile Co-Flex NL 4" - Product Usage: Single Use secondary wound dressing or compression wrap

Andover Healthcare Inc.

FDA Devices Moderate Oct 30, 2019

Torrent Suite Dx Software Version (IUO) 5.4 Catalog Number: A31774 OEM Customer Software: Sentosa SQ Suite Software v5.6.15

Life Technologies Holdings Pte Ltd

FDA Devices Moderate Oct 30, 2019

Canister HFC-134a / 980g, ALUM Product Number: 1600-00-0223 Revision .0C Coolant canister for use with surgical laser.

Candela Corporation

FDA Devices Moderate Oct 30, 2019

xTAG Respiratory Viral Panel (RVP): Box Label: xTAG RVP (Respiratory Viral Panel). Catalogue Number:I019C0111 in vitro diagnostic test

Luminex Molecular Diagnostics

FDA Devices Moderate Oct 30, 2019

Ergo 3.2mm K-wire - Product Usage: The devices is used assist the surgeon in the implantation of Equinoxe Shoulder System components according to a conventional technique for total shoulder replacement. The wire is single-use, provided sterile, and intended for transient use.

Exactech, Inc.

FDA Devices Moderate Oct 30, 2019

Rifton E-Pacer, SKU K660, powered lift device

Community Products, LLC

FDA Devices Moderate Oct 30, 2019

Plum 360 Infusion System With MedNet/ Smart Card Plug And Play Module, Model # 30010. Infusion pump.

ICU Medical Inc

FDA Devices Moderate Oct 30, 2019

Beckman Coulter Lipase, REF OSR6130 and OSR6230.

Beckman Coulter Inc.

FDA Devices Moderate Oct 30, 2019

Torrent Suite Dx Software Version 5.6.4 Catalog Number:A33178 OEM Customer software: Sentosa SQ Suite Software v5.6.20 UDI: (01)10190302005654 (11)000000 (10)5.6.4 (240)A33178

Life Technologies Holdings Pte Ltd

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.