PlainRecalls

2023 Recalls

6,617 recalls · Page 62 of 133

2023 Recall Year Insight

Federal agencies issued 6,617 product recalls indexed by PlainRecalls in calendar year 2023. That represents about 6.51% of the 101,704 total recalls we track from 1995 through the present, and averages roughly 18.1 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 133 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 2023.

On this page of 50 records, severity classification shows 9 critical, 40 moderate, and 1 lower-severity recalls. The page references 17 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 2023 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 Jul 12, 2023

Betta Link LG Reusable ProngED Guide - Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or…

T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.

FDA Devices Moderate Jul 12, 2023

OmniTom/OmniTom Elite- X-ray computed tomography applications for anatomy that can be imaged in the 40 cm aperture, primarily head and neck Model Nu…

NeuroLogica Corporation

FDA Devices Moderate Jul 12, 2023

SurgiMend 3.0; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 5x6 cm, 6x12 cm, 10x15 cm, 16x20 cm, 13x25 cm, 25x40 cm, 20x30 cm, 20x2…

TEI Biosciences, Inc.

FDA Devices Critical Jul 12, 2023

TruSignal AllFit Sensor: a) REF TS-AF-10, 10 pcs; B) REF AF-25, 25 pcs; Oximeter

GE Healthcare Finland Oy

FDA Devices Moderate Jul 12, 2023

SurgiMend 1.0; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 18x12 cm Thin and 10x15 cm Thin.

TEI Biosciences, Inc.

FDA Devices Moderate Jul 12, 2023

PriMatrix Fenestrated; Dermal Repair Scaffold; Rx Only; Sizes 4x4 cm, 6x6 cm, 8x8 cm, 14mm Disc, 18mm Disc, 2x2 cm, and 10x25 cm (Meshed 2:1).

TEI Biosciences, Inc.

FDA Devices Critical Jul 12, 2023

TruSignal Integrated Ear Sensor with Ohmeda Connector REF TS-E4-H; Oximeter

GE Healthcare Finland Oy

FDA Devices Moderate Jul 12, 2023

Aptio Automation Storage and Retrieval Module (SRM)

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Jul 12, 2023

Pilling LOWSLEY PROSTATIC TRACTOR CVD, REF 243200; retractor

TELEFLEX LLC

FDA Devices Moderate Jul 12, 2023

Custom medical procedure packs labeled as: a) CATH ANGIOGRAPHY DRAPE PACK, REF 89-7102; b) CHOLANGIOGRAPHY KIT, REF 89-7322; c) CATH LAB PAC…

DeRoyal Industries Inc

FDA Devices Moderate Jul 12, 2023

BETTA LINK SR KNOTLESS IMPLANT KIT-Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to …

T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.

FDA Devices Moderate Jul 12, 2023

Pilling O'REILLY ESOPHAGEAL RETRACTOR, REF 381801A; ENT retractor

TELEFLEX LLC

FDA Devices Moderate Jul 12, 2023

da Vinci Xi/X Tip-Up Fenestrated Grasper, REF: 470347, VER: 12

Intuitive Surgical, Inc.

FDA Devices Moderate Jul 12, 2023

TRACKMASTER, TREADMILL GE T2100-ST2 220V CHINA, MODEL NUMBER 317-07927GE CHINA

Full Vision Inc

FDA Devices Moderate Jul 12, 2023

Custom medical procedure packs labeled as: a) OPEN HEART TRACECART, REF '53-1941; b) CARDIAC CATH PACK, REF '89-10045; c) SHOULDER PACK, RE…

DeRoyal Industries Inc

FDA Devices Moderate Jul 12, 2023

PriMatrix Ag; Dermal Repair Scaffold; Rx Only; Sizes 10x12 cm, 10x25 cm, 20x25 cm, 4x4 cm, 6x6 cm, 8x12 cm, 8x8 cm.

TEI Biosciences, Inc.

FDA Devices Moderate Jul 12, 2023

TRACKMASTER, TREADMILL TMX428CP 220V, MODEL NUMBER 317-07929

Full Vision Inc

FDA Devices Moderate Jul 12, 2023

BD Synapsys Informatics Solution, Catalog Number 444150

Becton Dickinson & Co.

FDA Devices Moderate Jul 12, 2023

Custom medical procedure packs labeled as: a) STURDI STRAINER TRAY STANDARD, REF '89-5014

DeRoyal Industries Inc

FDA Devices Moderate Jul 12, 2023

Pilling LOWSLEY PROSTATIC TRACTOR STR, REF 243201; retractor

TELEFLEX LLC

FDA Devices Critical Jul 12, 2023

TruSignal Integrated Ear Sensor with Datex Connector, REF TS-E4-GE; Monitor, physiological, patient(with arrhythmia detection or alarms)

GE Healthcare Finland Oy

FDA Devices Moderate Jul 12, 2023

PriMatrix; Dermal Repair Scaffold; Rx Only; Sizes 0.2x26.5 cm (3 pack), 10x12cm, 10x25 cm, 20x25 cm, 4x4 cm, 6x6 cm, 8x12 cm, and 8x8 cm.

TEI Biosciences, Inc.

FDA Devices Moderate Jul 12, 2023

PriMatrix Ag Fenestrated; Dermal Repair Scaffold; Rx Only; Sizes 10x25 cm, 20x25 cm, 4x4 cm, 6x6 cm, 8x12 cm, 8x8 cm.

TEI Biosciences, Inc.

FDA Devices Moderate Jul 12, 2023

TRACKMASTER, TREADMILL TMX428 110V, MODEL NUMBER 317-07926

Full Vision Inc

FDA Devices Moderate Jul 12, 2023

Revize; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 10x10 cm, 4x12 cm, 4x16 cm.

TEI Biosciences, Inc.

FDA Devices Moderate Jul 12, 2023

Revize-X; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 12x6 cm and 10x9 cm.

TEI Biosciences, Inc.

FDA Devices Moderate Jul 12, 2023

SurgiMend MP; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 10x15 cm, 20x20 cm, 13x25 cm, 16x20 cm, 20x25 cm, 20x30 cm, and 25x40 cm.

TEI Biosciences, Inc.

FDA Devices Moderate Jul 12, 2023

Custom medical procedure packs labeled as: a) PELVIC EXAM TRAY, REF 89-6219

DeRoyal Industries Inc

FDA Devices Moderate Jul 12, 2023

SurgiMend; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 1.0 5x6 cm, 1.0 6x12 cm, 1.0 10x10 cm, 1.0 10x15 cm, 1.0 10x20 cm, 1.0 16x2…

TEI Biosciences, Inc.

FDA Devices Moderate Jul 12, 2023

SurgiMend 4.0; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 5x6 cm, 6x12 cm, 10x15 cm, 13x25 cm, 25x40 cm, 20x30 cm, 10x25 cm, 20x0…

TEI Biosciences, Inc.

FDA Devices Moderate Jul 12, 2023

PriMatrix Meshed; Dermal Repair Scaffold; Rx Only; Sizes 20x25 cm (1:1), 3x3 cm (2:1), 4x4 cm (2:1), 5x5 cm (2:1), 6x6 cm (2:1), 8x12 cm (2:1), and 8…

TEI Biosciences, Inc.

FDA Devices Moderate Jul 12, 2023

Custom medical procedure packs labeled as: a) STANDARD OB PACK ASCENSION WI, REF 89-10640 b) ANGIO PACK, REF 89-10901 c) BASIN, REF 89-1924 d) …

DeRoyal Industries Inc

FDA Devices Moderate Jul 12, 2023

KLS Martin Battery Pack, REF: KLS BP 001, and KLS BP 040 (bulk case of 40), used in conjunction with the KLS Martin MaxDriver

Pro-Dex Inc

FDA Devices Moderate Jul 12, 2023

Giraffe OmniBed Carestation CS1, Model Numbers: a. 2082844-001-XXX, b. 2074920-001-XXXXXX, c. M1050205, d. M1135822, e. M1145475, f. M1145476…

DATEX--OHMEDA, INC.

FDA Devices Critical Jul 12, 2023

TruSignal Adult/Pediatric Sensor; Oximeter, Ear: a) REF TS-AP-10, 10 pcs; b) REF TS-AP-25, 25 pcs

GE Healthcare Finland Oy

FDA Devices Moderate Jul 12, 2023

LinkSymphoKnee Distal Femoral Augment - Tilastan - Size. 7-8, Lateral-Right/Medial-Left, 5mm-Intended for primary and revision total knee replacement…

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Moderate Jul 12, 2023

BD Pyxis CII Safe, Software: V7, REF: 107-96, 107-97, 107-97-201; BD Pyxis CII Safe, Software: V7, REF: 107-223, 107-224, 111-191, 111-192, 111-193, …

CareFusion 303, Inc.

FDA Devices Critical Jul 12, 2023

Quidel Triage Cardiac Panel: REF: 97000HS, 97021HS (Troponin I), 97022HS (CK-MB and Troponin I), 97000HSEU, 97000HSEUJP, 97000HZ01, 97000QIL. Lots T1…

QUIDEL CARDIOVASCULAR INC

FDA Devices Moderate Jul 12, 2023

Trilogy Evo, Evo Clinical Korean (1137823) and Evo Caregiver Korean (1137853) Instructions for Use

Philips Respironics, Inc.

FDA Devices Moderate Jul 12, 2023

SurgiMend 2.0; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 5x6 cm, 6x12 cm, 10x15 cm, 16x20 cm, 13x25 cm, 25x40 cm, 20x30 cm, 20x2…

TEI Biosciences, Inc.

FDA Devices Low Jul 12, 2023

NeuMoDx SARS-CoV-2 Assay -IVD intended for the qualitative detection of SARS-CoV-2 RNA from nasal, nasopharyngeal and oropharyngeal swabs in transpo…

NeuMoDx Molecular Inc

FDA Devices Moderate Jul 12, 2023

Beside panel FRU (Field Replacement Units) Kits

DATEX--OHMEDA, INC.

FDA Devices Critical Jul 12, 2023

TruSignal Wrap Sensor, REF TS-W-D; Oximeter

GE Healthcare Finland Oy

FDA Devices Moderate Jul 12, 2023

TRACKMASTER, TREADMILL GE T2100-ST2 220V, MODEL NUMBER 317-07927GE

Full Vision Inc

FDA Devices Critical Jul 12, 2023

TruSignal Integrated Ear Sensor with Datex Connector, REF TS-E4-N; Oximeter

GE Healthcare Finland Oy

FDA Devices Critical Jul 12, 2023

TruSignal Integrated Ear Sensor with GE Connector REF TS-E2-GE; Oximeter, Ear

GE Healthcare Finland Oy

FDA Devices Moderate Jul 12, 2023

TissueMend; Advanced Soft Tissue Repair Matrix; Rx Only; Sizes 5x6 cm, 6x10 cm, and 3x3 cm.

TEI Biosciences, Inc.

FDA Devices Moderate Jul 12, 2023

Giraffe OmniBed, with the following Model Numbers: 6650-0004-901, 6650-0001-901, 6650-0003-901, 6650-0002-901, 6650-0094-901, 6650-0001-9901, 6650-00…

DATEX--OHMEDA, INC.

FDA Devices Critical Jul 12, 2023

TruSignal Ear Sensor, REF TS-E-D; Oximeter

GE Healthcare Finland Oy

FDA Devices Moderate Jul 12, 2023

TRACKMASTER, TREADMILL GE T2100-ST1 110VV, MODEL NUMBER 317-07926GE

Full Vision Inc

Nearby Recall Years

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

Compare 2023 with 2022 →

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 2023

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 2023 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.