PlainRecalls

2022 Recalls

5,888 recalls · Page 50 of 118

2022 Recall Year Insight

Federal agencies issued 5,888 product recalls indexed by PlainRecalls in calendar year 2022. That represents about 5.79% of the 101,704 total recalls we track from 1995 through the present, and averages roughly 16.1 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 118 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 1 critical, 44 moderate, and 5 lower-severity recalls. The page references 21 distinct recalling firms operating in 2 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (45), FDA Drug (5), 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, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Drug Moderate Jul 27, 2022

Launch Sequence Capsules, Dietary Supplement, 60- count bottles, ASIN B07TLPWXDS, UPC Code 641378938375.

Loud Muscle Science

FDA Drug Moderate Jul 27, 2022

0.9% Buffered Lidocaine HCl (buffered in 8.4% Sodium Bicarbonate), 45 mg/5 mL (9 mg/mL) syringes, packaged in 5 x 5 mL Prefilled Syringes per carton,…

Nephron Sterile Compounding Center LLC

FDA Drug Moderate Jul 27, 2022

Launch Sequence Euphoria Capsules, 10- count tins, ASIN B08ZJX4V9J, UPC Code 661020846864.

Loud Muscle Science

FDA Drug Moderate Jul 27, 2022

Anticoagulant Sodium Citrate Solution, USP 4%, 200 mg/5 mL (40 mg/mL) syringe, packaged in 5 x 5 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Car…

Nephron Sterile Compounding Center LLC

FDA Drug Moderate Jul 27, 2022

Neostigmine Methylsulfate Injection, USP, 3 mg/3 mL (1 mg/mL) syringe, packaged in 5 x 3 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per …

Nephron Sterile Compounding Center LLC

FDA Devices Moderate Jul 27, 2022

BD Connecta Stopcock Without Extension Tube Catalog No. 394601 (OUS)

Becton Dickinson & Company

FDA Devices Moderate Jul 27, 2022

AESCULAP S4 Cervical Cross Connector L24mm, S4C CROSS CONNECTOR FIXED 24MM, product code SWT113T. Used in spinal fusion surgery.

Aesculap Implant Systems LLC

FDA Devices Moderate Jul 27, 2022

SIGNA Premier magnetic resonance scanner, model 5748519.

GE Healthcare, LLC

FDA Devices Moderate Jul 27, 2022

SurgiCount+ System Application, Software Version 2.0.17, Catalog Number 0694-002-090. Used for counting, displaying, recording and locating the numb…

Stryker Instruments Div. of Stryker Corporation

FDA Devices Moderate Jul 27, 2022

ATTUNE Measured Sizing and Rotation Guide-to size the femur and align rotation of the bone cuts in preparation for the femoral implant Part Number: …

DePuy Orthopaedics, Inc.

FDA Devices Moderate Jul 27, 2022

BD Connecta Stopcock Without Extension Tube Catalog No. 394600 (OUS)

Becton Dickinson & Company

FDA Devices Low Jul 27, 2022

Soluble Transferrin Receptors (STFR), Catalog Number TF10159 (Research Use Only). IVD

Randox Laboratories Ltd.

FDA Devices Moderate Jul 27, 2022

ENDURO SPECIAL KEY TIB.LOCK.RING F1/10MM product code NP462R used with EnduRo Total Knee System. instrument used during orthopedic implant surgery.

Aesculap Implant Systems LLC

FDA Devices Moderate Jul 27, 2022

Sensis with software version VD12A. A diagnostic and administrative tool supporting hemodynamic catheterizations and/or electrophysiology studies, …

Siemens Medical Solutions USA, Inc

FDA Devices Low Jul 27, 2022

NeuRx Diaphragm Pacing System (NeuRx DPS), Affected part numbers: Part # Part Name 20-0035 NeuRx DPS System Kit 20-0036 …

Synapse Biomedical Inc

FDA Devices Moderate Jul 27, 2022

MODULIFT VBR SZ.M 4MM SET SCREW DRIVER, MF790R, part of Modulift VBR Medium Instrument Set, ST-0441

Aesculap Implant Systems LLC

FDA Devices Moderate Jul 27, 2022

Nexiva with Single BD Connecta Stopcock Version (Pink) Catalog No. 383687 (OUS)

Becton Dickinson & Company

FDA Devices Moderate Jul 27, 2022

LumiraDx SARS-CoV-2 Antibody (Ab) Liquid Quality Control

LumiraDx

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 #7142016…

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, 412391…

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 s…

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)…

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

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: CPSC + NHTSA - consumer product and vehicle recall feeds for 2022

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 2022 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 July 2026.