PlainRecalls

2022 Recall Year Insight

Federal agencies issued 5,957 product recalls indexed by PlainRecalls in calendar year 2022. That represents about 5.70% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 16.3 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 120 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 2022.

On this page of 50 records, severity classification shows 3 critical, 43 moderate, and 4 lower-severity recalls. The page references 23 distinct recalling firms operating in 2 distinct product categories, with 47 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (47), NHTSA (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 2022 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 Devices Critical Jul 27, 2022

GE Healthcare Aisys CS2 Anesthesia System, Part number 1011-9050-000; and Avance CS2 and Avance CS2 Pro Anesthesia System, Part number 1009-9050-000.

GE Healthcare, LLC

FDA Devices Moderate Jul 27, 2022

(1) Genesis II Non-Porous Tibial Baseplate Size 5 Right, Product #71420186. (2) Genesis II Non-Porous Tibial Baseplate Size 4 Left, Product #71420166.

Smith & Nephew, Inc.

FDA Devices Low Jul 27, 2022

Soluble Transferrin Receptors Calibrator Series (STFR CAL), Catalog Number TF10161. IVD

Randox Laboratories Ltd.

FDA Devices Moderate Jul 27, 2022

LifeGlobal Fast Freeze Thawing Kit, Model No. GFT5-055

CooperSurgical, Inc.

FDA Devices Moderate Jul 27, 2022

Hill-Rom PRO+ 36" MRS Surface With X-Ray mattress, REF P7924A01; and REF P7924ARENT01, PRO+ MRS Rental Surface with X-Ray mattress.

Baxter Healthcare Corporation

FDA Devices Moderate Jul 27, 2022

Hill-Rom PRO+ MRS Surface For Versacare With X-Ray mattress, REF P3255A01.

Baxter Healthcare Corporation

FDA Devices Moderate Jul 27, 2022

Ambu VivaSight 2 DLT; endobronchial tube system used for verifying tube placement and repositioning. Catalog numbers 412351000, 412371000, 412391000, 412411000

Ambu Inc.

FDA Devices Moderate Jul 27, 2022

BD Connecta White 360 Shelf 100Ea Catalog No. 395000 (OUS)

Becton Dickinson & Company

FDA Devices Moderate Jul 27, 2022

AESCULAP S4 Cervical Cross Connector L 42-58mm, S4C CROSS CONNECTOR VARIABLE 42-58MM, product code SW117T. Used in spinal fusion surgery.

Aesculap Implant Systems LLC

FDA Devices Moderate Jul 27, 2022

RIGHT CORONAL BENDER, TEK1940. Instrument used during spinal surgery.

Aesculap Implant Systems LLC

FDA Devices Moderate Jul 27, 2022

BD Connecta Stopcock Without Extension Tube Catalog No. 394602 (OUS)

Becton Dickinson & Company

FDA Devices Low Jul 27, 2022

Quantikine IVD Erythropoietin Human Serum Controls for use as quantitative controls for the determination of Erythropoietin concentrations in human serum and plasma. IFU, Part Number 750095

R & D Systems, Inc.

FDA Devices Moderate Jul 27, 2022

Nonsterile convenience kits: (1) regard Item #830099008, CV01005H - CV Part 1 Bundle; and (2) regard Item #830019017, CV00214Q - CV.

ROi CPS LLC

FDA Devices Moderate Jul 27, 2022

Nexiva with Single BD Connecta Stopcock Version (20 Ga Blue) Catalog No.383682 (OUS)

Becton Dickinson & Company

FDA Devices Moderate Jul 27, 2022

AESCULAP S4 Cervical Cross Connector L 33-42mm, S4C CROSS CONNECTOR VARIABLE 33-42MM, product code SW116T. Used in spinal fusion surgery.

Aesculap Implant Systems LLC

FDA Devices Moderate Jul 27, 2022

AESCULAP S4 Cervical Cross Connector L 28-33mm, S4C CROSS CONNECTOR VARIABLE 28-33MM, SW115T. Used in spinal fusion surgery.

Aesculap Implant Systems LLC

FDA Devices Moderate Jul 27, 2022

Triton Canister System (finished part numbers FG 12009, for 3L canisters, and FG 12019 for 2L canisters) Scanning Label (component part number 11032). A software application used to help estimation of blood loss. Used with blood bearing canisters and accessories.

Stryker Instruments Div. of Stryker Corporation

FDA Devices Moderate Jul 27, 2022

BD Connecta" Plus1 360 Blue Blend Catalog No. 394911 (OUS)

Becton Dickinson & Company

FDA Devices Moderate Jul 27, 2022

Hill-Rom Centrella Pro+ 40" Surface mattress, REF P7923A04.

Baxter Healthcare Corporation

FDA Devices Moderate Jul 27, 2022

Hobbs Medical Polypectomy Snare, Catalog No. 7202

Hobbs Medical, Inc.

FDA Devices Moderate Jul 27, 2022

RayStation 9B SP1. For radiation treatment planning.

RAYSEARCH LABORATORIES AB

FDA Devices Moderate Jul 27, 2022

LumiraDx SARS-CoV-2 Antibody (Ab) Test Strip

LumiraDx

FDA Devices Moderate Jul 27, 2022

BD Connecta" Plus3 White Blend OEM (sterile, bulk) Catalog No. 395214 (OUS)

Becton Dickinson & Company

FDA Devices Moderate Jul 27, 2022

SX-One MicroKnife

SONEX HEALTH LLC

FDA Devices Moderate Jul 27, 2022

Universal Robot UR5 arm, PV010204 subcomponent of Aesculap Aeos Digital Microscope System, PV010

Aesculap Implant Systems LLC

FDA Devices Moderate Jul 27, 2022

BD Connecta Stopcock Without Extension Tube Catalog No. 394605 (OUS)

Becton Dickinson & Company

FDA Devices Moderate Jul 27, 2022

BD Connecta 3-Way Stopcocks Catalog No. 394900 (OUS)

Becton Dickinson & Company

FDA Devices Moderate Jul 27, 2022

Nonsterile convenience kit: regard Item #830014016, LD00199P - C Section Mother.

ROi CPS LLC

FDA Devices Moderate Jul 27, 2022

GE Healthcare Avance CS2, Avance CS2 Pro Anesthesia Systems, Part #1009-9050-000; and Aisys CS2 Anesthesia Systems, Part # 1011-9050-000.

GE Healthcare, LLC

FDA Devices Moderate Jul 27, 2022

Hill-Rom Centrella Pro+ 36" Surface mattress, REF P7923A03.

Baxter Healthcare Corporation

FDA Devices Low Jul 27, 2022

Triton Sponge System (Software), GAUS-3, Software Versions 4.6.5, 4.8.7, 4.9.6

Stryker Instruments Div. of Stryker Corporation

FDA Devices Moderate Jul 27, 2022

X80 RADiant Photoelectric Therapy System

Xstrahl Limited

FDA Devices Moderate Jul 27, 2022

Hill-Rom Centrella Pro+ 36" Surface With X-Ray mattress, REF P7923A01.

Baxter Healthcare Corporation

FDA Devices Low Jul 27, 2022

GreenLight HPSEA Laser Fibers, UPN 0010-2092

Boston Scientific Corporation

FDA Devices Moderate Jul 27, 2022

ENNOVATE MIS REMOVALKEY SHORT, product code SZ380R

Aesculap Implant Systems LLC

FDA Devices Moderate Jul 27, 2022

Hill-Rom PRO+ MRS Surface For Versacare mattress, REF P3255A02.

Baxter Healthcare Corporation

FDA Devices Moderate Jul 27, 2022

YelloPort Elite Universal Seal. For use in laparoscopic procedures.

Surgical Innovations Ltd

FDA Devices Moderate Jul 27, 2022

LEFT CORONAL BENDER, TEK1939. Instrument used during spinal surgery.

Aesculap Implant Systems LLC

FDA Devices Moderate Jul 27, 2022

Hill-Rom PRO+ 36" MRS Surface mattress, REF P7924A03.

Baxter Healthcare Corporation

FDA Devices Moderate Jul 27, 2022

Sensis Vibe Combo with software version VD12A. A diagnostic and administrative tool supporting hemodynamic catheterizations and/or electrophysiology studies, for cardiac as well as interventional Radiology Model: 11007642

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 27, 2022

ENNOVATE MIS REMOVALKEY SHORT, product code SZ380R

Aesculap Implant Systems LLC

FDA Devices Moderate Jul 27, 2022

Trevo Trak 21 Microcatheter, REF: 90338. TREVO NXT 3X32+TRAK21 2-PACK - CE, REF: 91412; TREVO NXT 4X28+TRAK21 2-PACK - CE, REF: 91413; TREVO NXT 4X41+TRAK21 2-PACK - CE, REF: 91414; TREVO NXT 6X37+TRAK21 2-PACK - CE, REF: 91415; TREVO NXT 4X28+TRAK21+CAT6 3-PACK - CE, REF: SFP914170 TREVO NXT 6X37+TRAK21+CAT6 3-PACK - CE, REF: SFP914190. Used in the placement of devices and/or fluids, such as contrast media, into the peripheral, coronary, and neuro vasculature during diagnostic and/or

Stryker Neurovascular

FDA Devices Moderate Jul 27, 2022

BD Connecta Stopcock with OFF Directed Tap Without Extension Tube (500 eaches/carton) Catalog No. 394910 (US)

Becton Dickinson & Company

FDA Devices Moderate Jul 27, 2022

Randox Cholesterol- For the quantitative in vitro determination of Cholesterol in serum and plasma. Catalog Number: CH2O0

Randox Laboratories Ltd.

FDA Devices Moderate Jul 27, 2022

AESCULAP S4 Cervical Cross Connector L22mm, S4C CROSS CONNECTOR FIXED 22MM, product code SW112T. Used in spinal fusion surgery.

Aesculap Implant Systems LLC

FDA Devices Moderate Jul 27, 2022

AESCULAP S4 Cervical Cross Connector, L26mm, S4C CROSS CONNECTOR FIXED 26MM, product code SW114T. Used in spinal fusion surgery.

Aesculap Implant Systems LLC

FDA Devices Moderate Jul 27, 2022

Aesculap Sterile disposable fleece drape, Product code: GA414, individually packaged, 50 pieces per shipping unit, product code SZ380R.

Aesculap Implant Systems LLC

NHTSA No agency class Jul 27, 2022

AUDI,VOLKSWAGEN 2016: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE

AUDI,VOLKSWAGEN

NHTSA No agency class Jul 27, 2022

VOLKSWAGEN 2022: VISIBILITY:SUN/MOON ROOF ASSEMBLY

VOLKSWAGEN

NHTSA No agency class Jul 27, 2022

BMW 2022-2023: ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY

BMW

Nearby Recall Years

Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.

Compare 2022 with 2021 →

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 2022

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 2022 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.