2022 Recalls
5,957 federal recalls indexed for 2022 · Page 51 of 120
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.
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
(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.
Soluble Transferrin Receptors Calibrator Series (STFR CAL), Catalog Number TF10161. IVD
Randox Laboratories Ltd.
LifeGlobal Fast Freeze Thawing Kit, Model No. GFT5-055
CooperSurgical, Inc.
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
Hill-Rom PRO+ MRS Surface For Versacare With X-Ray mattress, REF P3255A01.
Baxter Healthcare Corporation
Ambu VivaSight 2 DLT; endobronchial tube system used for verifying tube placement and repositioning. Catalog numbers 412351000, 412371000, 412391000, 412411000
Ambu Inc.
BD Connecta White 360 Shelf 100Ea Catalog No. 395000 (OUS)
Becton Dickinson & Company
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
RIGHT CORONAL BENDER, TEK1940. Instrument used during spinal surgery.
Aesculap Implant Systems LLC
BD Connecta Stopcock Without Extension Tube Catalog No. 394602 (OUS)
Becton Dickinson & Company
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.
Nonsterile convenience kits: (1) regard Item #830099008, CV01005H - CV Part 1 Bundle; and (2) regard Item #830019017, CV00214Q - CV.
ROi CPS LLC
Nexiva with Single BD Connecta Stopcock Version (20 Ga Blue) Catalog No.383682 (OUS)
Becton Dickinson & Company
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
AESCULAP S4 Cervical Cross Connector L 28-33mm, S4C CROSS CONNECTOR VARIABLE 28-33MM, SW115T. Used in spinal fusion surgery.
Aesculap Implant Systems LLC
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
BD Connecta" Plus1 360 Blue Blend Catalog No. 394911 (OUS)
Becton Dickinson & Company
Hill-Rom Centrella Pro+ 40" Surface mattress, REF P7923A04.
Baxter Healthcare Corporation
Hobbs Medical Polypectomy Snare, Catalog No. 7202
Hobbs Medical, Inc.
RayStation 9B SP1. For radiation treatment planning.
RAYSEARCH LABORATORIES AB
LumiraDx SARS-CoV-2 Antibody (Ab) Test Strip
LumiraDx
BD Connecta" Plus3 White Blend OEM (sterile, bulk) Catalog No. 395214 (OUS)
Becton Dickinson & Company
SX-One MicroKnife
SONEX HEALTH LLC
Universal Robot UR5 arm, PV010204 subcomponent of Aesculap Aeos Digital Microscope System, PV010
Aesculap Implant Systems LLC
BD Connecta Stopcock Without Extension Tube Catalog No. 394605 (OUS)
Becton Dickinson & Company
BD Connecta 3-Way Stopcocks Catalog No. 394900 (OUS)
Becton Dickinson & Company
Nonsterile convenience kit: regard Item #830014016, LD00199P - C Section Mother.
ROi CPS LLC
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
Hill-Rom Centrella Pro+ 36" Surface mattress, REF P7923A03.
Baxter Healthcare Corporation
Triton Sponge System (Software), GAUS-3, Software Versions 4.6.5, 4.8.7, 4.9.6
Stryker Instruments Div. of Stryker Corporation
X80 RADiant Photoelectric Therapy System
Xstrahl Limited
Hill-Rom Centrella Pro+ 36" Surface With X-Ray mattress, REF P7923A01.
Baxter Healthcare Corporation
GreenLight HPSEA Laser Fibers, UPN 0010-2092
Boston Scientific Corporation
ENNOVATE MIS REMOVALKEY SHORT, product code SZ380R
Aesculap Implant Systems LLC
Hill-Rom PRO+ MRS Surface For Versacare mattress, REF P3255A02.
Baxter Healthcare Corporation
YelloPort Elite Universal Seal. For use in laparoscopic procedures.
Surgical Innovations Ltd
LEFT CORONAL BENDER, TEK1939. Instrument used during spinal surgery.
Aesculap Implant Systems LLC
Hill-Rom PRO+ 36" MRS Surface mattress, REF P7924A03.
Baxter Healthcare Corporation
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
ENNOVATE MIS REMOVALKEY SHORT, product code SZ380R
Aesculap Implant Systems LLC
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
BD Connecta Stopcock with OFF Directed Tap Without Extension Tube (500 eaches/carton) Catalog No. 394910 (US)
Becton Dickinson & Company
Randox Cholesterol- For the quantitative in vitro determination of Cholesterol in serum and plasma. Catalog Number: CH2O0
Randox Laboratories Ltd.
AESCULAP S4 Cervical Cross Connector L22mm, S4C CROSS CONNECTOR FIXED 22MM, product code SW112T. Used in spinal fusion surgery.
Aesculap Implant Systems LLC
AESCULAP S4 Cervical Cross Connector, L26mm, S4C CROSS CONNECTOR FIXED 26MM, product code SW114T. Used in spinal fusion surgery.
Aesculap Implant Systems LLC
Aesculap Sterile disposable fleece drape, Product code: GA414, individually packaged, 50 pieces per shipping unit, product code SZ380R.
Aesculap Implant Systems LLC
AUDI,VOLKSWAGEN 2016: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE
AUDI,VOLKSWAGEN
VOLKSWAGEN 2022: VISIBILITY:SUN/MOON ROOF ASSEMBLY
VOLKSWAGEN
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.
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.