PlainRecalls

2019 Recalls

7,480 recalls · Page 76 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 0 critical, 47 moderate, and 3 lower-severity recalls. The page references 15 distinct recalling firms operating in 1 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (50), 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 Devices Moderate Jul 31, 2019

Merge OrthoPACS versions 7.3, 7.3.1, 8.0 and 8.0.1

Merge Healthcare, Inc.

FDA Devices Moderate Jul 31, 2019

Terumo Sur-vet Needle, 20G x 1", Product Code 100204

Terumo Medical Corporation

FDA Devices Moderate Jul 31, 2019

3mL Luer-Lok Syringe, Catalog Number 309657, UDI 30382903096573

Becton Dickinson & Company

FDA Devices Moderate Jul 31, 2019

AXIOM Artis FA, Model Number 5904441

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 31, 2019

Monoject Standard Hypodermic Needle, 20 G x 1-1/2" bulk Item code: 8881200664

Cardinal Health 200, LLC

FDA Devices Moderate Jul 31, 2019

Monoject Standard Hypodermic Needle, 27 G x 1-1/4" Item code: 8881200508

Cardinal Health 200, LLC

FDA Devices Moderate Jul 31, 2019

Artis zee floor MN, Model Number 10094142

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 31, 2019

MAC VU360, Model Number 2030360-001, Electrocardiograph

GE Healthcare, LLC

FDA Devices Moderate Jul 31, 2019

Monoject Standard Hypodermic Needle Item code: 8881200029

Cardinal Health 200, LLC

FDA Devices Moderate Jul 31, 2019

C4 is an in vitro diagnostic assay for the quantitative determination of C4 in human serum or plasma. Antigen in the sample bonds to the specific an…

Abbott Laboratories, Inc

FDA Devices Low Jul 31, 2019

ARCHITECT BNP Calibrators Ptoduct Usage: The ARCHITECT BNP Calibrators are for the calibration of the ARCHITECT iSystem when used for the quantit…

Abbott Laboratories

FDA Devices Moderate Jul 31, 2019

Monoject Standard Hypodermic Needle, 16 G x 1-1/2" Item code:8881200045

Cardinal Health 200, LLC

FDA Devices Moderate Jul 31, 2019

MOOG Curlin Infusion Administration Set, REF 340-4130, Non-DEHP Tubing with Non-Vented Bag Spike and Vented 0.2 Micron Filter, packaged 20 sets/carto…

Zevex Incorporated (dba MOOG Medical Devices Group)

FDA Devices Moderate Jul 31, 2019

AXIOM Artis dMP, Model Number 7555365

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 31, 2019

Versa - Kath Mini Kit, with plastic L.O.R Syringe 12g X 12in (30.5 cm), 5 units, Sterile ED, REF 181-2112, RX, (01) 108187880213945, LOT 31129344 …

Epimed International, Inc.

FDA Devices Moderate Jul 31, 2019

AXIOM Artis dBC, Model Number 7728392

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 31, 2019

POWERPORT CLEARVUE isp, 6F CHRONOFLEX Catheter, Intermediate NAUTILUS DELTA Kit; POWERPORT CLEARVUE isp, 8F CHRONOFLEX Catheter, Intermediate NAUT…

Bard Peripheral Vascular Inc

FDA Devices Moderate Jul 31, 2019

Artis zee ceiling, Model Number 10094137

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 31, 2019

Monoject Blunt Cannula, 16 G x 1-1/2" (1.651 mm x 3.8 cm) Item code: 8881202322

Cardinal Health 200, LLC

FDA Devices Moderate Jul 31, 2019

GammaPod Stereotactic Radiotherapy System Model A, REF XMSGP030A00-0.02 Product Usage: GammaPod is a teletherapy device intended for use in the …

Xcision Medical Systems, LLC

FDA Devices Moderate Jul 31, 2019

Monoject Standard Hypodermic Needle, 14 G x 1-1/2" Item code: 8881200011

Cardinal Health 200, LLC

FDA Devices Low Jul 31, 2019

ARCHITECT BNP Controls Ptoduct Usage: The ARCHITECT BNP Controls are for the estimation of test precision and the detection of systematic analy…

Abbott Laboratories

FDA Devices Moderate Jul 31, 2019

STANLEY Healthcare Arial 54315 Network Manager

Stanley Security Solutions Inc

FDA Devices Moderate Jul 31, 2019

AXIOM Artis dBA, Model Number 7555357

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 31, 2019

AXIOM Artis dFA, Model Number 7555373

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 31, 2019

Terumo Sur-vet Needle, 22G x 1", Product Code 100211

Terumo Medical Corporation

FDA Devices Moderate Jul 31, 2019

Artis zee floor, Model Number 10094135

Siemens Medical Solutions USA, Inc

FDA Devices Low Jul 31, 2019

Breast Milk Transfer Lid for use with Oral Syringe Connectors Model: 90003S-100

Medela Inc

FDA Devices Moderate Jul 31, 2019

Terumo Sur-vet Needle, 22G x 3/4", Product Code 100215

Terumo Medical Corporation

FDA Devices Moderate Jul 31, 2019

3mL Safety-Lok Syringe, Catalog Number 309606, UDI 30382903096061

Becton Dickinson & Company

FDA Devices Moderate Jul 31, 2019

Immunoglobulin M is an in vitro diagnostic assay for the quantitative determination of immunoglobulin M in human serum or plasma. Antigen in the sam…

Abbott Laboratories, Inc

FDA Devices Moderate Jul 31, 2019

AXIOM Artis dTA, Model Number 7008605

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 31, 2019

Apolipoprotein A1 is an in vitro diagnostic assay for the quantitative determination of apolipoprotein A1 in human serum or plasma. Antibodies to ap…

Abbott Laboratories, Inc

FDA Devices Moderate Jul 31, 2019

Artis zee biplane, Model Number 10094141

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 31, 2019

Monoject Blunt Cannula, 22 G x 1-1/2" (0.711 mm x 3.8 cm) Item code: 8881202389

Cardinal Health 200, LLC

FDA Devices Moderate Jul 31, 2019

Versa - Kath Mini Kit, with plastic L.O.R Syringe 12g X 12in (30.5 cm), 5 units, Sterile ED, REF 181-2112, RX, (01) 108187880213945, LOT 311291155 …

Epimed International, Inc.

FDA Devices Moderate Jul 31, 2019

Immunoglobulin A is an in vitro diagnostic assay for the quantitative determination of immunoglobulin A in human serum or plasma. Antigen in the sam…

Abbott Laboratories, Inc

FDA Devices Moderate Jul 31, 2019

Artis zeego, Model Number 10280959

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 31, 2019

Terumo Needle, 18G x 1", Product Code NN1825R

Terumo Medical Corporation

FDA Devices Moderate Jul 31, 2019

Monoject 201 Vet Pak Hypodermic Needle, 19 ga x 1-1/2 Item code: 8881201522

Cardinal Health 200, LLC

FDA Devices Moderate Jul 31, 2019

Monoject 201 Vet Pak Hypodermic Needle, 22 ga x 1-1/2" Item code: 8881201456

Cardinal Health 200, LLC

FDA Devices Moderate Jul 31, 2019

Merge PACS versions 7.3, 7.3.1, 8.0 and 8.0.1

Merge Healthcare, Inc.

FDA Devices Moderate Jul 31, 2019

Immunoglobulin G is an in vitro diagnostic assay for the quantitative determination of immunoglobulin G in human serum or plasma. Antigen in the sam…

Abbott Laboratories, Inc

FDA Devices Moderate Jul 31, 2019

Artis zee multi, Model Number 10094139

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 31, 2019

Monoject 201 Vet Pak Hypodermic Needle, 20 ga x 1-1/2" Item code: 8881201498

Cardinal Health 200, LLC

FDA Devices Moderate Jul 31, 2019

Apolipoprotein B is an in vitro diagnostic assay for the quantitative determination of apolipoprotein B in human serum or plasma. Antibodies to apol…

Abbott Laboratories, Inc

FDA Devices Moderate Jul 31, 2019

Spacelabs Healthcare Smart Disclosure System, Model 92810, a component of the Intesys Clinical Suite (ICS) G2.

Spacelabs Healthcare, Inc.

FDA Devices Moderate Jul 31, 2019

Terumo Needle, 30G x 1/2", Product Code NN3013R

Terumo Medical Corporation

FDA Devices Moderate Jul 31, 2019

AXIOM Artis TA, Model Number 7007755

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 31, 2019

AXIOM Artis dFC, Model Number 7727717

Siemens Medical Solutions USA, 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 August 2026.