PlainRecalls

2022 Recalls

4,921 recalls · Page 5 of 99

2022 Recall Year Insight

Federal agencies issued 4,921 product recalls indexed by PlainRecalls in calendar year 2022. That represents about 5.86% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 13.5 recalls per day across the FDA, CPSC, NHTSA, and USDA FSIS 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 99 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 7 critical, 43 moderate, and 0 lower-severity recalls. The page references 6 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 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, NHTSA, or USDA FSIS for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Devices Moderate Dec 21, 2022

DeRoyal BIOPSY PACK, REF 89-9739.05

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

DeRoyal ENDOVASCULAR TRACEPACK, REF 89-9350.03

DeRoyal Industries Inc

FDA Devices Critical Dec 21, 2022

Arrow AutoCAT2 Intra-Aortic Balloon Pump, AC3 IABP NA/AJLA, REF IAP-0601(IPN916548), cardiac pump

ARROW INTERNATIONAL Inc.

FDA Devices Moderate Dec 21, 2022

BASIC IMPLANT PACK, Item No. 40310SBI, oral surgery tray

Stradis Medical, LLC dba Stradis Healthcare

FDA Devices Moderate Dec 21, 2022

DeRoyal CATARACT PACK, REF 89-8650.10

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

Surgical room, SURGICAL PACK, Item No.40996WLS, oral surgery tray

Stradis Medical, LLC dba Stradis Healthcare

FDA Devices Moderate Dec 21, 2022

HENRY SCHEIN, CATH ANGIO PACK, Item No.570-2930

Stradis Medical, LLC dba Stradis Healthcare

FDA Devices Moderate Dec 21, 2022

DeRoyal CATARACT PACK, REF 89-8859.08

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

HENRY SCHEIN, Knee Pack, Item No.570-2908,

Stradis Medical, LLC dba Stradis Healthcare

FDA Devices Moderate Dec 21, 2022

DeRoyal CNRV SPINAL PACK, REF 89-10532.03

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

DeRoyal HEART PACK, REF 89-8351.13

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests (600T)- US. Siemens Material Number (SMN): 10708840 For in vitro diagnostic use w…

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Dec 21, 2022

DeRoyal BASIC NEURO PACK, REF 89-7523.16

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

DeRoyal ACDF PACK PGYBK A PACK / B PACK, REF 89-9997.06

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

NUVASIVE MAGEC MAGEC 2 Rod. The MAGEC System is used to brace the spine during growth to minimize the progression of scoliosis. REF Model Numb…

NuVasive Specialized Orthopedics, Inc.

FDA Devices Critical Dec 21, 2022

Arrow AC3 Optimus Intra-Aortic Balloon Pump, AC3 Optimus IABP NA/AJLA, REF IAP-0701 (IPN917286), cardiac pump

ARROW INTERNATIONAL Inc.

FDA Devices Moderate Dec 21, 2022

GEO-MED CATARACT PACK, REF 89-5790.08

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

DeRoyal SHOULDER ARTHOSCOPY PACK, REF 89-10820.02

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

DeRoyal TLIF PACK, REF 89-8780.04

DeRoyal Industries Inc

FDA Devices Critical Dec 21, 2022

Arrow AC3 Optimus Intra-Aortic Balloon Pump, AC3 Optimus IABP NA/EMEA, REF IAP-0700(IPN917285), cardiac pump

ARROW INTERNATIONAL Inc.

FDA Devices Moderate Dec 21, 2022

DeRoyal ACDF PACK, REF 89-8779.03

DeRoyal Industries Inc

FDA Devices Critical Dec 21, 2022

Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500E (IPN000322), cardiac pump

ARROW INTERNATIONAL Inc.

FDA Devices Moderate Dec 21, 2022

DeRoyal ORTHO SPINE BACK PACK, REF 89-7534.09

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

HENRY SCHEIN, TEMP STIMULATOR SUPPLIES, Item No.570-2883

Stradis Medical, LLC dba Stradis Healthcare

FDA Devices Moderate Dec 21, 2022

DeRoyal BREAST AUGMENTATION PACK, REF 89-9618.05

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

DeRoyal PODIATRY PACK, REF 89-8359.13

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

STRADIS HEALTHCARE, Varicosity Basic Pack, Item No.682-947,

Stradis Medical, LLC dba Stradis Healthcare

FDA Devices Moderate Dec 21, 2022

HENRY SCHEIN, BONE MARROW KIT, Item No.570-3092

Stradis Medical, LLC dba Stradis Healthcare

FDA Devices Moderate Dec 21, 2022

DeRoyal LAMINECTOMY SPINAL FUSION PACK, REF 89-9105.09

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

DeRoyal FOOT PACK, REF 89-9252.07

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

ARTISTE, ONCOR and PRIMUS with syngo RT Therapist with software version 4.3.1 MR3. Material Number: 8162815 Intended Use: Family of linear acc…

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Dec 21, 2022

STRADIS HEALTHCARE, Breast, Item No.693-276,

Stradis Medical, LLC dba Stradis Healthcare

FDA Devices Moderate Dec 21, 2022

ACE Surgical Supply, 17539 CUSTOM KIT STERILE Item No.003-3880, oral surgery tray

Stradis Medical, LLC dba Stradis Healthcare

FDA Devices Moderate Dec 21, 2022

DeRoyal NEURO SPINE BACK PACK PGYBK, REF 89-10853.01

DeRoyal Industries Inc

FDA Devices Critical Dec 21, 2022

Arrow AutoCAT2 Intra-Aortic Balloon Pump, AC3 IABP NA/AJLA, REF IAP-0601(IPN917288), cardiac pump

ARROW INTERNATIONAL Inc.

FDA Devices Moderate Dec 21, 2022

STRADIS HEALTHCARE, Medical Vein, Item No.682-330,

Stradis Medical, LLC dba Stradis Healthcare

FDA Devices Moderate Dec 21, 2022

DeRoyal LAMINECTOMY SPINAL FUSION PACK, REF 89-9105.10

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

DeRoyal NEURO PACK, REF 89-9253.07

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

DeRoyal HAND PACK, REF 89-10314.03

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

STRADIS HEALTHCARE, Vasc Vein, Item No.682-1583,

Stradis Medical, LLC dba Stradis Healthcare

FDA Devices Moderate Dec 21, 2022

DeRoyal PAIN TRAY, REF 89-10464.02

DeRoyal Industries Inc

FDA Devices Critical Dec 21, 2022

Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500D (IPN000321), cardiac pump

ARROW INTERNATIONAL Inc.

FDA Devices Moderate Dec 21, 2022

DeRoyal PICC LINE TRAY PGYBK, REF 89-6150.13

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

GEO-MED TOTAL KNEE PACK A & B, REF 89-6799.02

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

STRADIS HEALTHCARE, COTTON APPLICATOR 3" Item No.505-010,

Stradis Medical, LLC dba Stradis Healthcare

FDA Devices Moderate Dec 21, 2022

DeRoyal CARDIAC LINEN PACK, REF 89-10543.02

DeRoyal Industries Inc

FDA Devices Critical Dec 21, 2022

Arrow AutoCAT 2 Intra-Aortic Balloon Pump, Arrow AutoCAT 2 IABP, REF IAP-0400F (IPN000306), cardiac pump

ARROW INTERNATIONAL Inc.

FDA Devices Moderate Dec 21, 2022

HENRY SCHEIN, PROCEDURE TRAY, Item No.570-2900,

Stradis Medical, LLC dba Stradis Healthcare

FDA Devices Moderate Dec 21, 2022

DeRoyal SHOULDER PACK, REF 89-9449.12

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

DeRoyal CANNULTED HIP PACK CSM, REF 89-6977.09

DeRoyal Industries Inc

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 + USDA FSIS — consumer product, vehicle, and meat/poultry recall feeds for 2022