PlainRecalls

2019 Recalls

Compiled from official public sources by the editorial team.

7,480 recalls · Page 25 of 150

2019 Recall Year Insight

Federal agencies issued 7,480 product recalls indexed by PlainRecalls in calendar year 2019. That represents about 7.35% of the 101,704 total recalls we track from 1995 through the present, and averages roughly 20.5 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 150 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 1 critical, 49 moderate, and 0 lower-severity recalls. The page references 16 distinct recalling firms operating in 3 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (44), 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, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Drug Moderate Nov 13, 2019

S-ESTRADIOL VALERATE 20MG/ML MDV INJ IN ETHYL OLEATE, packaged in a) 5ml, b) 10ml, glass vial, RX Only, Red Mountain Compounding RX.

First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

FDA Drug Moderate Nov 13, 2019

S-ATROPINE 0.5% OPTH SOLN, 10 ML dropper bottle, RX only, Red Mountain Compounding RX.

First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

FDA Drug Moderate Nov 13, 2019

Basic Reset CBD Reset 2400, True Full Spectrum Natural (unflavored), 2400 mg CBD, 1 fl. oz. (29 mL) bottle, Distributed by: Basic Reset Hendersonvill…

Basic Reset Inc.

FDA Drug Moderate Nov 13, 2019

S-AMITRIPTYLINE 10MG/ML MDV INJ SOLN, 30ML, glass vial, Rx Only, Red Mountain Compounding RX

First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

FDA Drug Moderate Nov 13, 2019

S-TRIMIX (40MG/2.5MG/29MCG) MDV INJ; Rx Only, 5ml glass vial, Red Mountain Compounding Rx

First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

FDA Drug Moderate Nov 13, 2019

S-TESTOSTERONE CYP 200MG/ML MDV In SESAME OIL, Rx Only, a) 5ML, b) 10ML, c) 13 ML glass vial, Red Mountain Compounding Rx

First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

FDA Devices Moderate Nov 13, 2019

(1) Argon Medical Devices Vascuclamp, Radiopaque Vascular Clamp, Small Straight, REF 046-1-200, 2 clamps/package, 5 packages/box, 10 boxes/case, Ster…

Argon Medical Devices, Inc

FDA Devices Moderate Nov 13, 2019

BF Humeral Stem, Various Sizes, Item Nos. 00430000606 00430000613 00430000706 00430000713 00430000813 00430000817 00430000820 00430000913 004…

Zimmer Biomet, Inc.

FDA Devices Moderate Nov 13, 2019

Connection Screw for NCB Plate, Item No. 0202266002

Zimmer Biomet, Inc.

FDA Devices Moderate Nov 13, 2019

StemPro¿ MSC SFM CTS"

Life Technologies Corporation

FDA Devices Moderate Nov 13, 2019

Liquid Protein Calibrators (SP CAL (LIQ)) Catalogue Number: IT2691 GTIN: 05055273204032 Product Usage: Liquid Protein Calibrators are intended for…

Randox Laboratories Ltd.

FDA Devices Moderate Nov 13, 2019

Prismaflex Control Unit, software versions below 7.21

Baxter Healthcare Corporation

FDA Devices Moderate Nov 13, 2019

PERIARTICULAR PLATES - FEMUR, Item Nos. 00234700106 00234700108 00234700110 00234700112 00234700114 00234700116 00234700118 00234700206 00234…

Zimmer Biomet, Inc.

FDA Devices Moderate Nov 13, 2019

Prismaflex Control Unit, software versions below 7.21

Baxter Healthcare Corporation

FDA Devices Moderate Nov 13, 2019

Various Knee Systems, Item Nos. 32855411838 32855411840 32855411842 32855411843 32855420307 32855420308 32855420309 32855420310 32855420315 …

Zimmer Biomet, Inc.

FDA Devices Critical Nov 13, 2019

Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 for use with ventilators.

TELEFLEX-MORRISVILLE

FDA Devices Moderate Nov 13, 2019

Argon Medical Devices TRI-JECT, 3 Way IV Administration Organizer without Stopcock, REF 041230001A, 25/box, Sterile, Rx. The firm name on the label …

Argon Medical Devices, Inc

FDA Devices Moderate Nov 13, 2019

Prox Lat Tib Lock Plate and Dist Med Tib Lock Plate Item Nos. 47235700306 47235700308 47235700310 47235700312 47235700314 47235700408 472357…

Zimmer Biomet, Inc.

FDA Devices Moderate Nov 13, 2019

Metasul Femoral Heads, various sizes, Item Nos. 00877004001 00877004002 00877004003 00877004004 00877004005

Zimmer Biomet, Inc.

FDA Devices Moderate Nov 13, 2019

Prismaflex Control Unit, software versions below 7.21

Baxter Healthcare Corporation

FDA Devices Moderate Nov 13, 2019

NCB PERIPROSTHETIC, "NCB PP PROX FEM PLATE", Various sizes, Item Nos. 0202263009 0202263012 0202263015 0202263018 0202263021 0202263109 0202263…

Zimmer Biomet, Inc.

FDA Devices Moderate Nov 13, 2019

Autoject EI, REF AJ1310

Owen Mumford USA, Inc.

FDA Devices Moderate Nov 13, 2019

Various temporary devices used during the implantation of the device system: bone fixation plates and screws, drill bits, manual surgical instruments…

Zimmer Biomet, Inc.

FDA Devices Moderate Nov 13, 2019

Prismaflex Control Unit, software versions below 7.21

Baxter Healthcare Corporation

FDA Devices Moderate Nov 13, 2019

VITROS chemistry Products Cl- Slides, Catalog No. 8445207 (which does NOT support Urine CL-). MicroSlides which contain reagents in a dry, multi-laye…

Ortho-Clinical Diagnostics

FDA Devices Moderate Nov 13, 2019

(1) Argon Medical Devices Double Female LL Adapter, Special Adapter to Convert a Male Fitting to Female LL, REF 040183000A, 25/box, Sterile, Rx; and …

Argon Medical Devices, Inc

FDA Devices Moderate Nov 13, 2019

Ceramic Femoral Heads, various sizes, Item Nos. 00877504001 00877504002 00877504003 00877504004

Zimmer Biomet, Inc.

FDA Devices Moderate Nov 13, 2019

Various fixation systems and accessories, Item Nos. 00118100522 00118100527 00118100530 00118100532 00118100535 00118100537 00118100540 001181…

Zimmer Biomet, Inc.

FDA Devices Moderate Nov 13, 2019

PROX LAT HUMERAL LOCK PLATE, Item Nos. 47235800104 47235800106 47235800108 47235800112 47235800116 47235800204 47235800206 47235800208 472358…

Zimmer Biomet, Inc.

FDA Devices Moderate Nov 13, 2019

Various fixation systems and accessories, Item Nos. 00224000916 00224000918 00224000920 00224000922 00224000924 00224000926 00224000928 002240…

Zimmer Biomet, Inc.

FDA Devices Moderate Nov 13, 2019

VITROS chemistry Products K+ Slides, Catalog No. 8157596. MicroSlides which contain reagents in a dry, multi-layered form.

Ortho-Clinical Diagnostics

FDA Devices Moderate Nov 13, 2019

LPS-MOB ART SURF IMPL D 9MM

Zimmer Biomet, Inc.

FDA Devices Moderate Nov 13, 2019

The LivaNova VNS Therapy System, used for Vagus Nerve Stimulation (VNS), consists of an implantable VNS Therapy generator, lead, and external program…

LivaNova USA Inc

FDA Devices Moderate Nov 13, 2019

Low Level Output Cable Interface to Philips Monitor For Use With Cardiosave and CS300 Intra-Aortic Balloon Pumps (IABPs), Part Number 0012-00-1589…

Datascope Corp.

FDA Devices Moderate Nov 13, 2019

ZPLP Fibular Plate, Item Nos. 00234701504 00234701506 00234701508 00234701510 00234701512 00234701516 00234701604 00234701606 00234701608 00…

Zimmer Biomet, Inc.

FDA Devices Moderate Nov 13, 2019

Grab n Go Opti series VIPR system Model # PRX-9646 - Product Usage: The Grab n Go Opti system is an integrated delivery system intended to provide …

Western / Scott Fetzer Company

FDA Devices Moderate Nov 13, 2019

Argon Medical Devices Double Male LL Adapter, REF 040184800A, bulk, non-sterile. The firm name on the label is Argon Medical Devices, Inc., Athens, …

Argon Medical Devices, Inc

FDA Devices Moderate Nov 13, 2019

Universal Locking Plates Sterile, Item Nos. 47492800207 47492800303 47492800402 47492800403 47492800407 47492800502 47492800503 47492800507 …

Zimmer Biomet, Inc.

FDA Devices Moderate Nov 13, 2019

Various Knee Systems for knee joint arthroplasty, knee prosthesis, Item Nos. 00522000100 00522000200 00522000300 00522000400 00522006304 0052200…

Zimmer Biomet, Inc.

FDA Devices Moderate Nov 13, 2019

Periarticular Plates - Tibial, Item Nos. 00234700304 00234700306 00234700308 00234700310 00234700312 00234700314 00234700316 00234700404 0023…

Zimmer Biomet, Inc.

FDA Devices Moderate Nov 13, 2019

Grab n Go Opti series VIPR system Model # PRX-9653 - Product Usage: The Grab n Go Opti system is an integrated delivery system intended to provide …

Western / Scott Fetzer Company

FDA Devices Moderate Nov 13, 2019

NCB-PH Plate with 4/5/7 Lock Holes, Item Nos. 0202262104 0202262105 0202262107

Zimmer Biomet, Inc.

FDA Devices Moderate Nov 13, 2019

SCFE (slipped capital femoral epiphysis) Knobs for Driver, 6.5mm and 7.3 mm Orthopedic surgical instrument component, for hip surgery

Pega Medical Inc.

FDA Devices Moderate Nov 13, 2019

Omnipod DASH Insulin Management System, Product Catalog Number 18239 M/D: PDM USA1 D001 MG USA1

Insulet Corporation

FDA Devices Moderate Nov 13, 2019

DIST LAT FEM LCK PLATE STERILE, Item Nos. 47235710106 47235710110 47235710114 47235710118 47235710122 47235710210 47235710214 47235710218 4…

Zimmer Biomet, Inc.

FDA Devices Moderate Nov 13, 2019

Prismaflex Control Unit, software versions below 7.21

Baxter Healthcare Corporation

FDA Devices Moderate Nov 13, 2019

Cephalomedullary Nail (CMN), Various sizes, Item Nos. 47249318009 47249318010 47249318011 47249318013 47249318014 47249318109 47249318110 4724…

Zimmer Biomet, Inc.

FDA Devices Moderate Nov 13, 2019

Centurion Medical Products UNIVERSAL LINE FULL BODY DRAPE KIT - REG Code: DT11955

Centurion Medical Products Corporation

FDA Devices Moderate Nov 13, 2019

Various Devices for Limb salvage arthroplasty, Item Nos. 00585000011 00585001201 00585001202 00585001301 00585001302 00585003038 00585003214 0…

Zimmer Biomet, Inc.

FDA Devices Moderate Nov 13, 2019

PERIARTICULAR PLATES SHOULDER, PERI PROX LAT HUMERAL, Item Nos. 00234800104 00234800106 00234800108 00234800110 00234800112 00234800114 0023480…

Zimmer Biomet, Inc.

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

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