PlainRecalls

2019 Recalls

7,396 recalls · Page 98 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 4 critical, 46 moderate, and 0 lower-severity recalls. The page references 9 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 May 29, 2019

Drill, 3.2x145mm, AO, Item Number ST502015650

Zimmer GmbH

FDA Devices Critical May 29, 2019

LimiTorr INS9020 INS-9020 LIMITORR VOLUME LIMITING EVD 20 ML LimiTorr INS9020SP1 INS-9020SP1 LIMITORR VOLUME EVD 20ML LimiTorr INS9030 INS-9030 LIM…

Integra LifeSciences Corp.

FDA Devices Moderate May 29, 2019

Thio Med w/Dex, Hem, Vit, K (7ml) 100/PK Product Usage; Recommended for use in qualitative procedures as a general purpose media for the cultiv…

Remel Inc

FDA Devices Moderate May 29, 2019

Drill, cannulated, 2x95mm, AO, Item Number 502015623

Zimmer GmbH

FDA Devices Moderate May 29, 2019

Thio Med w/Dex, Hem, Vit K(10ml) 100/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivati…

Remel Inc

FDA Devices Moderate May 29, 2019

Drill, cannulated, 3.5x90mm, round shaft, Item Number ST502015635

Zimmer GmbH

FDA Devices Moderate May 29, 2019

Drill, cannulated, 2.5x95mm, AO, Item Number ST502015621

Zimmer GmbH

FDA Devices Moderate May 29, 2019

Drill, contra-angle, 1.5x85mm, Item Number 502015706

Zimmer GmbH

FDA Devices Critical May 29, 2019

EV1000 Clinical Platform, Models: EV1000A, EV1000NI, EV1000CS Product Usage: EV1000A Monitor is used to optimize fluid management through the use…

Edwards Lifesciences, LLC

FDA Devices Moderate May 29, 2019

Drill, cannulated, 3x90mm, AO, Item Number 502015631

Zimmer GmbH

FDA Devices Moderate May 29, 2019

CBS micro, countersink, cannulated, AO, Item Number 503004541

Zimmer GmbH

FDA Devices Moderate May 29, 2019

AURIGA XL 4007 BRAZIL SYSTEM Model: M0068FS4007B0 Product Usage: The Auriga XL 4007 Laser System and the Auriga 30 Laser System including a …

Boston Scientific Corporation

FDA Devices Moderate May 29, 2019

Drill, cannulated, 3.5x90mm, round shaft, Item Number 502015635

Zimmer GmbH

FDA Devices Moderate May 29, 2019

AURIGA 30 BRAZIL SYSTEM UPN: M0068S30B0 Product Usage: The Auriga XL 4007 Laser System and the Auriga 30 Laser System including a fiber optic…

Boston Scientific Corporation

FDA Devices Moderate May 29, 2019

V-TEK", micro-countersink, round shaft, Item Number 28.66.112

Zimmer GmbH

FDA Devices Moderate May 29, 2019

Drill, cannulated, 2x95mm, round shaft, Item Number ST502015619

Zimmer GmbH

FDA Devices Moderate May 29, 2019

AURIGA 30 GENERAL SYSTEM UPN: M0068S30G0 Product Usage: The Auriga XL 4007 Laser System and the Auriga 30 Laser System including a fiber opti…

Boston Scientific Corporation

FDA Devices Moderate May 29, 2019

Drill Sys2.7, 2x103mm, AO, Item Number 502015107

Zimmer GmbH

FDA Devices Moderate May 29, 2019

Osteofresh arthrodesis drill, 2x70mm, center tip, AO, 10mm stop, Item Number 502015213

Zimmer GmbH

FDA Devices Moderate May 29, 2019

Thio Med w/o Ind, w/Dex (9ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation o…

Remel Inc

FDA Devices Moderate May 29, 2019

AURIGA XL 4007 GENERAL SYSTEM UPN: M0068FS4007G0 Product Usage: The Auriga XL 4007 Laser System and the Auriga 30 Laser System including a fi…

Boston Scientific Corporation

FDA Devices Moderate May 29, 2019

OAKWORKS Inc.Lithotripsy/Urology Table: CFLU401, Catalog Number: 75216-T01 - Product Usage: Oakworks¿ Imaging Tables are radiographic tables intended…

Oakworks Inc

FDA Devices Moderate May 29, 2019

Drill, cannulated, 4x90mm, round shaft, Item Number 502015640

Zimmer GmbH

FDA Devices Moderate May 29, 2019

Drill Sys 2.7, 2x105mm, stryker, Item Number 502015106

Zimmer GmbH

FDA Devices Moderate May 29, 2019

Drill, 2.5x94mm, Stryker, Item Number 502015136

Zimmer GmbH

FDA Devices Moderate May 29, 2019

V-TEK", standard-countersink, cannulated, AO, Item Number 28.66.111

Zimmer GmbH

FDA Devices Moderate May 29, 2019

Drill, 19mm stop, 1.9x87mm, AO, Item Number 502015131

Zimmer GmbH

FDA Devices Moderate May 29, 2019

Drill, 2.5x87mm, AO, Item Number 502015137

Zimmer GmbH

FDA Devices Moderate May 29, 2019

Drill, cannulated, 2x95mm, AO, Item Number ST502015623

Zimmer GmbH

FDA Devices Critical May 29, 2019

MoniTorr 10100 10-100 CSF Drainage System w/Patient Line One Way Valve MoniTorr 10102 10-102 CSF Drainage System w/Patient Line One Way Valve w Mon…

Integra LifeSciences Corp.

FDA Devices Moderate May 29, 2019

Neomem Resorbable Collagen Membrane, 15 mm x 20 mm Reference Number (model): N1520 - Product Usage: Neomem is a bioresorbable, implantable collagen …

Collagen Matrix, Inc.

FDA Devices Moderate May 29, 2019

Drill, 15mm stop, 1x76mm, AO , Item Number 502015115

Zimmer GmbH

FDA Devices Moderate May 29, 2019

Drill, cannulated, 4x150mm, AO, Item Number ST502015403

Zimmer GmbH

FDA Devices Moderate May 29, 2019

CBS micro, countersink, cannulated, AO, Item Number ST503004541

Zimmer GmbH

FDA Devices Critical May 29, 2019

UniCel DxH 900 Coulter Cellular Analysis System, REF number C11478 Product Usage: Note: The DxH 900 hematology analyzer is CLIA categorized under…

Beckman Coulter Inc.

FDA Devices Moderate May 29, 2019

Drill, cannulated, 3x90mm, round shaft, Item Number ST502015630

Zimmer GmbH

FDA Devices Moderate May 29, 2019

NeuViz 64 Multi-slice CT Scanner System Product Usage: The Multi-Slice CT Scanner System can be used as a whole body computed tomography x-ray sys…

Neusoft Medical Systems Co., Ltd.

FDA Devices Moderate May 29, 2019

AURIGA XL 4007 GENERAL - DEMO SYSTEM UPN: M0068FS4007GD0 Product Usage: The Auriga XL 4007 Laser System and the Auriga 30 Laser System includ…

Boston Scientific Corporation

FDA Devices Moderate May 29, 2019

Drill, 26mm stop, 1.9x94mm, Stryker, Item Number 502015130

Zimmer GmbH

FDA Devices Moderate May 29, 2019

Drill for 2.7mm screw, 20mm stop, 2x105mm, Stryker, Item Number 502015206

Zimmer GmbH

FDA Devices Moderate May 29, 2019

Drill for 2.7mm screw, 23mm stop, 2x103mm, AO, Item Number 502015207

Zimmer GmbH

FDA Devices Moderate May 29, 2019

Thio Med w/Dex, Hem, Vit K (7ml) 20/PK Product Usage; Recommended for use in qualitative procedures as a general purpose media for the cultivat…

Remel Inc

FDA Devices Moderate May 29, 2019

V-TEK", Micro-countersink, AO , Item Number ST28.66.113

Zimmer GmbH

FDA Devices Moderate May 29, 2019

V-TEK", standard-countersink, cannulated, AO, Item Number ST28.66.111

Zimmer GmbH

FDA Devices Moderate May 29, 2019

Thio Med w/o Ind, w/Dex (18ml) 100/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation…

Remel Inc

FDA Devices Moderate May 29, 2019

Drill, cannulated, 4x120mm, AO, Item Number 502015402

Zimmer GmbH

FDA Devices Moderate May 29, 2019

NeuViz 16 Essence Multi-slice CT Scanner System Product Usage: The Multi-Slice CT Scanner System can be used as a whole body computed tomography x…

Neusoft Medical Systems Co., Ltd.

FDA Devices Moderate May 29, 2019

Thio Med w/Dex, Hem, Vit K (9ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivatio…

Remel Inc

FDA Devices Moderate May 29, 2019

V-TEK", IVP step drill 2-3.4x124mm, 16mm stop, contra-angle, Item Number 502015634

Zimmer GmbH

FDA Devices Moderate May 29, 2019

Drill, cannulated, 2.5x95mm, round shaft, Item Number 502015620

Zimmer GmbH

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