PlainRecalls

2022 Recalls

Compiled from official public sources by the editorial team.

5,888 recalls · Page 7 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 9 critical, 41 moderate, and 0 lower-severity recalls. The page references 7 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, or NHTSA 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

GEO-MED SHOULDER ARTHROSCOPY KNEE PACK, REF 89-5797.09

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

DeRoyal MAJOR ORTHO PACK, REF 89-9250.07

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

Cordis Angiographic Catheter Extensions. Used to transport fluid from the power injector to the catheter for injection into the patient.

Cordis US Corp

FDA Devices Moderate Dec 21, 2022

DeRoyal EYE PACK, REF 89-8756.03

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

DeRoyal OPEN SHOULDER PROCEDURE PACK RF, REF 89-6629.07

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

STRADIS HEALTHCARE, pack Item No.40788SMS, oral surgery tray

Stradis Medical, LLC dba Stradis Healthcare

FDA Devices Moderate Dec 21, 2022

STRADIS HEALTHCARE, TIP, SURGE-O-VAC .125" GREEN, Item No.SS077225,

Stradis Medical, LLC dba Stradis Healthcare

FDA Devices Moderate Dec 21, 2022

DeRoyal EXTREMITY TRAY PGYBK, REF 89-4081.07

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

DeRoyal KIT HEART B PACK, REF 89-9042.08

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

DeRoyal EYE TRAY PGYBK, REF 89-7978.02

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

DeRoyal NEURO PACK, REF 89-10171.05

DeRoyal Industries Inc

FDA Devices Critical Dec 21, 2022

Arrow AutoCAT 2 Intra-Aortic Balloon Pump, Arrow AutoCAT 2 IABP, REF IAP-0400E (IPN000305), cardiac pump

ARROW INTERNATIONAL Inc.

FDA Devices Moderate Dec 21, 2022

DeRoyal ABDOMINOPLASTY W/LIPO PACK, REF 89-9557.03

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

DeRoyal TOTAL HIP KIT, REF 89-9498.10

DeRoyal Industries Inc

FDA Devices Critical Dec 21, 2022

Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit, REF numbers: a) ASK-42703-NS, b) ASK-42703-PCCH2, c) ASK-42703-PUPM1, d) ASK-45703-NS, …

ARROW INTERNATIONAL Inc.

FDA Devices Moderate Dec 21, 2022

DeRoyal TOTAL HIP PACK, REF 89-9301.07

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

DeRoyal SHOULDER ARTHOSCOPY PACK, REF 89-10061.02

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

STRADIS HEALTHCARE, Surgical Pk, Item No.40510TWS, oral surgery tray

Stradis Medical, LLC dba Stradis Healthcare

FDA Devices Moderate Dec 21, 2022

STRADIS HEALTHCARE, DENTAL CUSTOM PACK, Item No.41137TDS,

Stradis Medical, LLC dba Stradis Healthcare

FDA Devices Moderate Dec 21, 2022

STRADIS HEALTHCARE, Thoracic Phleb, Item No.682-1228,

Stradis Medical, LLC dba Stradis Healthcare

FDA Devices Moderate Dec 21, 2022

HENRY SCHEIN, GYN PACK, Item No.570-2625

Stradis Medical, LLC dba Stradis Healthcare

FDA Devices Moderate Dec 21, 2022

PDS II (polydioxanone) Suture- VIOLET MONOFILAMENT 27IN 0 S/A CT-1 Product Code: Z340H For use in soft tissue approximation, including use in ped…

Ethicon, Inc.

FDA Devices Moderate Dec 21, 2022

DeRoyal CATARACT PACK, REF 89-7135.10

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

DeRoyal CUSTOM NEURO PACK, REF 89-8392.10

DeRoyal Industries Inc

FDA Devices Critical Dec 21, 2022

Arrow MAC Two-Lumen Central Venous Access Kit fr use with 7 - 7.5 Fr Catheters, REF ASK-11242-UPM1; catheter introducer

ARROW INTERNATIONAL Inc.

FDA Devices Moderate Dec 21, 2022

DeRoyal SPINE PACK, REF 89-8361.10

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

STRADIS HEALTHCARE, Vein RF Pack, Item No.682-1942NL1,

Stradis Medical, LLC dba Stradis Healthcare

FDA Devices Moderate Dec 21, 2022

DeRoyal PACEMAKER ICD PACK, REF 89-10216.03

DeRoyal Industries Inc

FDA Devices Critical Dec 21, 2022

Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500J (IPN000325), cardiac pump

ARROW INTERNATIONAL Inc.

FDA Devices Moderate Dec 21, 2022

DeRoyal GU ROBOTIC PACK, REF 89-7063.12

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

GEO-MED PODIATRY PACK PGYBK, REF 89-8700.01

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

DeRoyal BREAST TRAY, REF 89-7033.07

DeRoyal Industries Inc

FDA Devices Critical Dec 21, 2022

Arrow AutoCAT2 Intra-Aortic Balloon Pump, AC3 IABP NA/EMEA, REF IAP-0600 (IPN917287), cardiac pump

ARROW INTERNATIONAL Inc.

FDA Devices Moderate Dec 21, 2022

DeRoyal BASIC NEURO PACK, REF 89-7258.12

DeRoyal Industries Inc

FDA Devices Critical Dec 21, 2022

Arrow AutoCAT2 Intra-Aortic Balloon Pump, AUTOCAT2 IAPB, REFURBISHED, REF IAP-0400X (IPN000311), cardiac pump

ARROW INTERNATIONAL Inc.

FDA Devices Moderate Dec 21, 2022

DeRoyal BASIC EYE PACK, REF 89-8337.08

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

DeRoyal SHOULDER KIT, REF 89-9497.10

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

DeRoyal GU PACK, REF 89-10665.02

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

GEO-MED OPTHALMOLOGY CSTM PCK, REF 89-6387.08

DeRoyal Industries Inc

FDA Devices Critical Dec 21, 2022

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

ARROW INTERNATIONAL Inc.

FDA Devices Moderate Dec 21, 2022

DeRoyal EMERGENT TRAUMA PACK, ref 89-9453.12

DeRoyal Industries Inc

FDA Devices Moderate Dec 21, 2022

STRADIS HEALTHCARE, Ablation Pack, Item No.682-130,

Stradis Medical, LLC dba Stradis Healthcare

FDA Devices Moderate Dec 21, 2022

DeRoyal BASIC PACK, REF 89-8633.07

DeRoyal Industries Inc

FDA Devices Critical Dec 21, 2022

Arrow AutoCAT2 Intra-Aortic Balloon Pump, AC3 IABP NA/AJLA, REF IAP-0601 (IPN001109), cardiac pump

ARROW INTERNATIONAL Inc.

FDA Devices Moderate Dec 21, 2022

HENRY SCHEIN, CUSTOM PK 2, Item No.570-3072

Stradis Medical, LLC dba Stradis Healthcare

FDA Devices Moderate Dec 21, 2022

NexGen Option Stemmed Tibial Component Size 3, Item Number 00-5986-037-01

Zimmer, Inc.

FDA Devices Moderate Dec 21, 2022

IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests OUS, except Japan Siemens Material Number (SMN): 10380875 For the quantitative…

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Dec 21, 2022

Surgical room, DENTAL SURGICAL PACK, Item No.41236SDSP

Stradis Medical, LLC dba Stradis Healthcare

FDA Devices Moderate Dec 21, 2022

DeRoyal TOTAL SHOULDER PACK, REF 89-10151.05

DeRoyal Industries Inc

FDA Devices Critical Dec 21, 2022

Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500J (IPN000334), cardiac pump

ARROW INTERNATIONAL 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 - 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.