PlainRecalls

2023 Recall Year Insight

Federal agencies issued 6,706 product recalls indexed by PlainRecalls in calendar year 2023. That represents about 6.42% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 18.4 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 135 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 8 critical, 41 moderate, and 1 lower-severity recalls. The page references 16 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, USDA FSIS, 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

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 PACK, REF 89-9183

DeRoyal Industries Inc

FDA Devices Moderate Jul 12, 2023

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, REF '89-10115; d) MINOR ORTHO PACK, REF '89-10213; e) TOTAL KNEE PACK PGYBK, REF '89-10505; f) ANTERIOR HIP PACK PGYBK, REF '89-10563; g) ORTHO X-RAY PACK, REF '89-1495; h) GU PACK, REF '89-4479; i) BREAST PACK, REF '89-5424; j) SHOULDER ARTHROSCOPY PK, REF '89-6606; k) GYN PACK, REF '89-7369; l) ENT PACK, REF '89-7378; m) TOTAL HI

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 16x20 cm, 1.0 13x25 cm, 1.0 4x16 cm, 1.0 3x3 cm, 1.0 4x7 cm, 1.0 4x12 cm, 1.0 6x16 cm, 1.0 25x40 cm, 1.0 20 x 30 cm, 1.0 8x16 cm, 1.0 4x7 cm Thin, 1.0 5x6 cm Thin, 1.0 3x3 cm Thin, 1.0 0.3x25 cm, 1.0 0.6x25 cm, 1.0 1x25 cm.

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, 20x0.5 cm, and 10x25 cm Fenestrated.

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 8x8 cm (2:1).

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) CYSTO PACK, REF 89-7133 e) TOTAL HIP PACK, REF 89-9134 f) EMERGENCY C-SECTION PACK, REF 89-9478

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, g. M1235957, h. M1149051, i. M1146098; Labeled as the following: GIRAFFE OMNIBED CARESTATION CS1, GIRAFFE OMNIBED CARESTATION, GIRAFFE OMNIBED, GIRAFFE OMNIBED CS1, OMNI G 115/230V SERVO2 CARESTATION, ASSY-LAU, OMNIBED CHINA EBASE S HUMID, Manufacturing assembly - Make, OBSOLETE-Omnibed Czech Servo O2 Nist/Scale/Re-usable Probe/SW w/port ho

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 in skeletally mature patients. Product Code: 880-307/21

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, 111-194, 111-195, 111-196, 111-197, 111-198; BD Pyxis CII Safe, Software: V8, 111-199-01, 111-200-01, 111-201-01, 111-202-01, 111-203-01, 111-204-01, 111-205-01, 111-206-01, 107-245-01, 107-246-01; BD Pyxis CII Safe, Software: V9, REF: 107-252-01, 111-215, 111-216, 111-219, 111-221. BD Pyxis CII Safe, Software: ES, REF: 107-254-01, 107-255-01, 1116-

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 T13664 - T14045.

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, 20x20 cm, 20x25cm, 10x15cm Semi-Oval,

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 transport medium and bronchoalveolar lavage (BAL) specimens from individuals suspected of COVID-19 by their healthcare provider (HCP). REF Number: 300800

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, 6650-0029-901, 6650-0080-901, 6650-0032-901, 6650-0077-901, 6650-001-901, 6650-0006-901, 6650-0129-901, 6650-0063-902, 6650-0130-901, 6650-0082-902, 6650-0061-902, 6650-0131-902, 6650-0034-902, 6650-0104-902, 6650-0066-902, 6650-0042-902, 6650-0143-901, 6650-0148-902, 6650-0152-901, 6650-0107-902, 6650-0136-902, 6650-0060-902, 6650-0056-902, 6650-0043-902.

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

FDA Devices Moderate Jul 12, 2023

TRACKMASTER, TREADMILL TMX428 220V, MODEL NUMBER 317-07927

Full Vision Inc

FDA Devices Moderate Jul 12, 2023

SurgiMend PRS; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 10x15 cm Semi-Oval, 7x17 cm Fenestrated, 10x20 cm Fenestrated, 8x16 cm Semi-Oval, 15x15 cm Semi-Oval, 8x20 cm Fenestrated, 10x15 cm Slant Fenestrated, 7x17 cm Semi-Oval, 8x16 cm Thin Semi-Oval, 10x20 cm Thin Semi-Oval, 6x16 cm Semi-Oval, Thin Oval 8x12 cm, Thin Oval 10x15 cm, Meshed 20cm x 10cm

TEI Biosciences, Inc.

FDA Devices Moderate Jul 12, 2023

TRACKMASTER, TREADMILL TMX428CP 110V, MODEL NUMBER 317-07928

Full Vision Inc

FDA Devices Moderate Jul 12, 2023

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

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: USDA FSIS Recalls - calendar-year meat, poultry, and processed egg product recall filings
  • Source: CPSC + NHTSA - consumer product and vehicle recall feeds for 2023

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 2023 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.