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 0 critical, 50 moderate, and 0 lower-severity recalls. The page references 17 distinct recalling firms operating in 2 distinct product categories, with 49 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (47), FDA Drug (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 Drug Moderate Dec 4, 2019

DG Health Acid Reducer Ranitidine Tablets 150 mg, 8-count carton, Distributed by: Dolgencorp LLC 100 Mission Ridge Goodletville TN 37072 NDC 55910-092-79

AuroMedics Pharma LLC

FDA Drug Moderate Dec 4, 2019

Ibuprofen Oral Suspension USP, 100 mg/5mL, 4 fl.oz. 118 mL, Rx only, Preferred Pharmaceuticals, Inc., Anaheim, CA. Mfg: Taro Pharm.; Hawthorne, NY; NDC 68788-7268-01

Preferred Pharmaceuticals, Inc

FDA Drug Moderate Dec 4, 2019

Testosterone Cypionate 180 mg/mL/Testosterone Propionate 20mg/mL Oil Injection Solution, 10 mL per vial, New Vitalis Pharmacy

New Vitalis Pharmacy LLC dba New Vitalis Pharmacy

FDA Devices Moderate Dec 4, 2019

Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 12cm UPN: M00536700

Boston Scientific Corporation

FDA Devices Moderate Dec 4, 2019

Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 5cm UPN: M00536630

Boston Scientific Corporation

FDA Devices Moderate Dec 4, 2019

Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 9cm UPN: M00536670

Boston Scientific Corporation

FDA Devices Moderate Dec 4, 2019

UniCel DxH Slidemaker Stainer (DxH SMS) and UniCel DxH Slidemaker Stainer II (DxH SMS II) - Product Usage: The intended use is as follows: The DxH Slidemaker Stainer is a fully automated slide preparation and staining device that aspirates a whole-blood sample, smears a blood film on a clean microscope slide, and delivers a variety of fixatives, stains, buffers, and rinse solutions to that blood smear.

Beckman Coulter, Inc.

FDA Devices Moderate Dec 4, 2019

ARCHITECT HAVAB-G Calibrator, REF 6L27-01

Abbott Gmbh & Co. KG

FDA Devices Moderate Dec 4, 2019

COMP RVRS Shoulder Baseplates, including Custom Products, Item numbers 115331S 115331 115330S 115330 110040610 110040620 010000589 CP561861 PM0001456 PM551047 PM551063 PM555137 PM555160 PM555209 PM555322 PM555406 PM555415 UDI: (01)00880304475342(17)211128(10)704850 (01)00880304475342(17)220128(10)094500 (01)00880304475342(17)220328(10)856620 (01)00880304475342(17)220528(10)487710 (01)00880304475342(17)220628(10)028860 (01)00880304475342(17)220628(10)028870 (01)0088030

Zimmer Biomet, Inc.

FDA Devices Moderate Dec 4, 2019

BIOMOD PORCOAT HA GLENTRAY; Custom Shoulder Products Item Nos. PM0000097 PM555140 PM555147 PM555319 PM555418 113867 113865 113863 Product Usage: Total Shoulder Replacement

Zimmer Biomet, Inc.

FDA Devices Moderate Dec 4, 2019

BALL NOSE GUIDE WIRE 80CM, 100CM. Item Nos. 281001080 281001100 Product Usage: These instruments and delivery systems are used to facilitate implantation of orthopedic medical devices.

Zimmer Biomet, Inc.

FDA Devices Moderate Dec 4, 2019

Various Hip systems, Item Nos. 104207 104212 104215 11-162809 11-162810 11-162811 11-162812 11-162813 21-103202 21-103203 21-103204 21-103205 21-103206 21-103207 21-103208 21-103209 21-103210 21-103211 21-103212 21-103215 21-104109 21-104110 21-104111 21-104112 21-104113 21-104114 21-104115 21-104116 21-104117 21-104118 21-104119 21-108110 21-108112 21-108115 21-108117 21-108119 21-108130 21-108132 21-108135 21-108137 21-108139 21-108150 21-108152 21-10

Zimmer Biomet, Inc.

FDA Devices Moderate Dec 4, 2019

Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 13cm UPN: M00536710

Boston Scientific Corporation

FDA Devices Moderate Dec 4, 2019

Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 10cm UPN: M005336680

Boston Scientific Corporation

FDA Devices Moderate Dec 4, 2019

Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 15cm UPN: M005337206

Boston Scientific Corporation

FDA Devices Moderate Dec 4, 2019

Boston Advanix Pancreatic Stent, Straight Leading Barb, 10F x 4cm UPN: M00536620

Boston Scientific Corporation

FDA Devices Moderate Dec 4, 2019

Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 3cm UPN: M00536610

Boston Scientific Corporation

FDA Devices Moderate Dec 4, 2019

HA Pins (DFS HA Cort Screw), Hoffman/Colles Pins (Colles CSER Sterile w/ Pin Kit) Item Nos: HAA60-09030 HAA60-09040 HAA60-10030 HAA60-10040 HAA60-11030 HAA60-11040 HAA60-11050 HAA60-12040 HAA60-12060 HAA60-13030 HAA60-13040 HAA60-13050 HAA60-13060 HAA60-13070 HAA60-14050 HAA60-14080 HAA60-14090 HAA60-15020 HAA60-15030 HAA60-15040 HAA60-15050 HAA60-15060 HAA60-16030 HAA60-16040 HAA60-16050 HAA60-16070 HAA60-16090 HAA60-17040 HAA60-17060 HAA60-17080 HAA60-18010 HA

Zimmer Biomet, Inc.

FDA Devices Moderate Dec 4, 2019

4Fr x 20cm Single Lumen CT Midline Basic Tray, Product Code: VYML4S1001

Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc.

FDA Devices Moderate Dec 4, 2019

Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 18cm UPN: M00536730

Boston Scientific Corporation

FDA Devices Moderate Dec 4, 2019

Comprehensive RS Cleat CAP, Item No. 110300

Zimmer Biomet, Inc.

FDA Devices Moderate Dec 4, 2019

PRO-STIM 10cc INJECTABLE, Part Number 86SR0410

Wright Medical Technology, Inc.

FDA Devices Moderate Dec 4, 2019

ACROMIUM FLANGE SET (Custom product) Item No. PM555148 - Product Usage: Arcomium replacement.

Zimmer Biomet, Inc.

FDA Devices Moderate Dec 4, 2019

Spectranetics AngioSculpt PTCA Scoring Balloon Catheter, balloon outer diameter 2.5mm, balloon length 15mm, REF 2027-2515, Sterile, Rx. The firm name on the label is Spectranetics Corporation, Fremont, CA.

Spectranetics Corporation

FDA Devices Moderate Dec 4, 2019

LT DISC ULNA - HA/PC; RT DISC ULNA - HA/PC; LT DISC HMRL- HA/PC; RT DISC HMRL- HA/PC; DISC XS ULNA POR; DISC SEG ULNA POR; and Custom devices Item Nos. 114754 114755 114744 114745 114704 114705 114756 114757 114714 114715 114746 114747 114706 114707 114758 114759 114716 114717 114748 114749 114708 114709 114718 114719 CP561429 CP561430 CP561431 CP561432 CP561442 CP561449 CP561488 CP561489 CP561709 CP561710 CP561714 CP561715 PM555203 Product Usage:

Zimmer Biomet, Inc.

FDA Devices Moderate Dec 4, 2019

Atellica CH 930 Analyzer

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Dec 4, 2019

Stratum Foot Plating System-NL LP Screw 3.5x50mm ST, sterile. Catalog Number: STRM-NL-3550ST - Product Usage: The Stratum Foot Plating System is a plate and screws construct indicated for fixation of fractures, osteotomies, nonunions, malunions and fusions of small bones and small bone segments, particularly in osteopenic bone.

Nextremity Solutions

FDA Devices Moderate Dec 4, 2019

HENNESSY LEFT CONST GLENOID HA, Item No. PM555360 UDI (01)00880304819597(17)260425(10)664030 Product Usage: Constrained Shoulder.

Zimmer Biomet, Inc.

FDA Devices Moderate Dec 4, 2019

Darco STERILE HEADED DRILL BIT 4.4MM , Part Number 777S06514

Wright Medical Technology, Inc.

FDA Devices Moderate Dec 4, 2019

SWANSON FINGER JOINT #1, Part Number 4700001

Wright Medical Technology, Inc.

FDA Devices Moderate Dec 4, 2019

INBONE STEM, TIBIAL, TOP, Part Number 200011901

Wright Medical Technology, Inc.

FDA Devices Moderate Dec 4, 2019

In-the-Ear hearing aids, Model Numbers: T9ITC-DW-LP, FT6ITC-D-MP, FT6ITE-D-MP, FT8CIC-MP, FT8ITC-W-HP, FT8ITC-W-LP, FT8ITC-W-MP, FT8ITE-DW-HP, FT8MIH-W-HP, FT8MIH-W-MP, LT5CIC-MP, LT5CIC-UP, LT5IIC-LP, LT5ITC-DW-MP, LT5ITC-DW-UP, LT5ITE-DW-HP, LT5ITE-DW-MP, LT5ITE-DW-UP, LT5MIH-W-HP, LT5MIH-W-MP, LT5MIH-W-UP, LT7CIC-HP, LT7CIC-LP, LT7CIC-MP, LT7CIC-W-MP, LT7IIC-LP, LT7ITC-DW-LP, LT7ITC-DW-MP, LT7ITC-MP, LT7ITC-W-HP, LT7ITC-W-MP, LT7ITE-DW-HP, LT7ITE-DW-MP, LT7ITE-DW-UP, LT7ITE-W-UP, LT7MIH-W-H

GN Hearing A/S

FDA Devices Moderate Dec 4, 2019

Various Custom Products, Item Nos. CP102940 CP102941 CP102942 CP102943 CP102944 CP102945 CP102946 CP102947 CP102948 CP112662 CP112663 CP112664 CP112674 CP112675 CP113771 CP113777 CP113778 CP113782 CP113783 CP114083 CP114090 CP114112 CP114118 CP114148 CP114213 CP114388 CP114436 CP114463 CP114472 CP114478 CP114495 CP114532 CP114561 CP114563 CP114605 CP114695 CP114756 CP114782 CP114783 CP114933 CP114987 CP115008 CP115048 CP115049 CP115050 CP115166 CP115

Zimmer Biomet, Inc.

FDA Devices Moderate Dec 4, 2019

myCordella Patient Kit without ECG, The Cordella System is a comprehensive at-home heart failure management platform that provides the clinician tools to monitor the progression of heart failure.

ENDOTRONIX

FDA Devices Moderate Dec 4, 2019

NC Emerge Monorail PTCA Dilatation Catheter. Sterilized using ethylene oxide. Packaged in the following sizes: 1. REF/Catalog No. H7493926708350, NC EMERGE MR US 3.50MM X 8MM; 2. REF/Catalog No. H7493927608350, NC EMERGE MR OUS 3.50MM X 8MM; 3. REF/Catalog No. H7493927608400, NC EMERGE MR OUS 4.00MM X 8MM; 4. REF/Catalog No. H7493927612200, NC EMERGE MR OUS 2.00MM X 12MM; 5. REF/Catalog No. H7493926712250, NC EMERGE MR US 2.50MM X 12MM; 6. REF/Catalog No. H7493927612250,

Boston Scientific Corporation

FDA Devices Moderate Dec 4, 2019

Rocket KCH Fetal Bladder Drainage Catheter Model: R57405

Rocket Medical Plc

FDA Devices Moderate Dec 4, 2019

CPS CALCANEAL PLATE SML 54MM, Part Number DCS2805001

Wright Medical Technology, Inc.

FDA Devices Moderate Dec 4, 2019

Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 11cm UPN: M005336690

Boston Scientific Corporation

FDA Devices Moderate Dec 4, 2019

Advanix Pancreatic Stent, Straight Leading Barb, 10F x 6cm UPN: M00536640

Boston Scientific Corporation

FDA Devices Moderate Dec 4, 2019

EVENCARE G3 Blood Glucose Test Strips, 1 test strip per foil pouch, 50 foil pouches per box, 12 boxes per case.

Medline Industries Inc

FDA Devices Moderate Dec 4, 2019

Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 7cm UPN: M00536650

Boston Scientific Corporation

FDA Devices Moderate Dec 4, 2019

EVANS OPENING WEDGE PLATE 10MM, Part Number 58S30010

Wright Medical Technology, Inc.

FDA Devices Moderate Dec 4, 2019

V-Twin, REF 6002-800 or 6002-850, SN 18-3304, IVD, (01)03661540600180

Vital Scientific N.V.

FDA Devices Moderate Dec 4, 2019

Guidezilla II Guide Extension Catheter Sterilized using ethylene oxide. Packaged in the following sizes: 1. REF/Catalog No. H7493933515060, 6F; 2. REF/Catalog No H7493933515070, 7F.

Boston Scientific Corporation

FDA Devices Moderate Dec 4, 2019

SWANSON TRAPEZIUM IMPLANT, Part Number 4520002

Wright Medical Technology, Inc.

FDA Devices Moderate Dec 4, 2019

SWANSON GREAT TOE, TITANIUM SZ 4, Part Number 4833104

Wright Medical Technology, Inc.

FDA Devices Moderate Dec 4, 2019

VALOR SCREW 5.0MM X 45MM LEN, Part Number 4151150045

Wright Medical Technology, Inc.

FDA Devices Moderate Dec 4, 2019

Accessory kit, Alinity i containing Alinity ci Level Sensor, Bulk Solution

Abbott Gmbh & Co. KG

FDA Devices Moderate Dec 4, 2019

ASI 2.0 Calcar Trimmer Shaft for Use with Biomet¿ Rasp, Model Number 110032331

Zimmer Biomet, Inc.

FDA Devices Moderate Dec 4, 2019

Compress, Mini Compress; Item Nos. 178350 178351 178352 178353 178354 178355 178356 178357 178358 178359 178360 178361 178362 178363 178364 178365 178366 178367 178368 178369 178370 178371 178372 178373 178464 178472 178480 178488 178496 178504 178575 178576 178577 178578 178579 178580 178730 178731 178732 178733 178734 178735 178354S 178754 178755 178756 178757 178758 178759 Product Usage: 1) Correction of revision of unsuccessful osteotomy, ar

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: 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.