PlainRecalls

2023 Recalls

6,535 recalls · Page 112 of 131

2023 Recall Year Insight

Federal agencies issued 6,535 product recalls indexed by PlainRecalls in calendar year 2023. That represents about 7.78% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 17.9 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 131 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, 41 moderate, and 0 lower-severity recalls. The page references 23 distinct recalling firms operating in 5 distinct product categories, with 45 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (41), NHTSA (5), CPSC (4), 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 Mar 8, 2023

Biofinity XR Toric 6-pack- Soft (hydrophilic) Contact Lens (extended wear)

CooperVision, Inc.

FDA Devices Moderate Mar 8, 2023

Surgilon Braided Nylon suture Product Description: 88861883-51 SURGILON* 2-0 BLK 75CM C16 88861915-71 SURGILON* 1 BLK 75CM GS11 88861919-31 SURGI…

Covidien, LP

FDA Devices Moderate Mar 8, 2023

Alaris PC Unit 8015 utilizing 802.11 b/g or 802.11 a/b/g wireless network cards, with IP addresses from x.x.x.224 to x.x.x.255

CareFusion 303, Inc.

FDA Devices Moderate Mar 8, 2023

Dermalon Monofilament Nylon Suture: (1) 88861741-11 DERMALON* 6-0 BLU 45CM C1 (2) 88861747-11 DERMALON* 6-0 BLU 45CM C12 (3) 88861749-24 DERMALO…

Covidien, LP

FDA Devices Moderate Mar 8, 2023

ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 40241425, Bone fixation device

Wright Medical Technology, Inc.

FDA Devices Moderate Mar 8, 2023

Custom Suture Pack Product Description: US1638 CUSTOM SUTURE PACK US1756 CUSTOM SUTURE PACK

Covidien, LP

FDA Devices Moderate Mar 8, 2023

BEQ-HLS 5050 USA; HLS Set Advanced 5.0, Product Code 70106.9077, BEQ-HLS 7050 USA; HLS Set Advanced 7.0, Product Code 70106.9078. Part of th…

Maquet Medical Systems USA

FDA Devices Critical Mar 8, 2023

Life2000 Ventilator PKG, Hospital, a) REF BT200011, b) REF BT-20-0011, ventilatory support for the care of individuals

Baxter Healthcare Corporation

FDA Devices Moderate Mar 8, 2023

Triton Canister Software Catalog Number: GAUS-2. Intended adjunct in the estimation of blood loss.

Stryker Corporation

FDA Devices Moderate Mar 8, 2023

Ti-Cron Coated Braided Polyester Suture Product Description 88862775-31 TICRON* 4-0 BLU 75CM CV327DA 88862880-41 TICRON* 3-0 WHI 75CM Y31DA 88863…

Covidien, LP

FDA Devices Moderate Mar 8, 2023

MultiLab Series II ROODRA non-invasive vascular diagnostic device, Model Number 11986-0000-01

Unetixs Vascular, Inc.

FDA Devices Moderate Mar 8, 2023

Surgidac Uncoated Braided Polyester suture Product Description D-1764K SURGIDAC* 5-0 WHI 45CM SS24DA

Covidien, LP

FDA Devices Moderate Mar 8, 2023

Phoenix mKDR Xpress, digital mobile diagnostic x-ray system

SEDECAL SA

FDA Devices Moderate Mar 8, 2023

Summit Medical Nasal Septal Button, Medium, 5cm, REF SP-78105, sterile.

Summit Medical, LLC

FDA Devices Moderate Mar 8, 2023

DRX-Compass/DR-FIT X-ray Systems with Firmware version 2.3.2.0/2.3.2.4. For use in obtaining diagnostic quality radiographic images to aid the physi…

Carestream Health, Inc.

FDA Devices Moderate Mar 8, 2023

Parietex Composite Mesh Polyester with Absorbable Collagen Film, Horseshoe- Shaped, 9 x 8 cm (3.6" x 3.1"). Intended for the reinforcement of tissue…

Covidien, LP

FDA Devices Moderate Mar 8, 2023

MultiLab Series II 2CP & 2CP Express non-invasive vascular diagnostic device, Model Number 11996-0000-01

Unetixs Vascular, Inc.

FDA Devices Moderate Mar 8, 2023

SciCan STATIS SL S10001 Dental Handpieces-Intended for the removal of carious material, reducing hard tooth structure, cavity preparation, finishing …

Coltene Whaledent Inc

FDA Devices Moderate Mar 8, 2023

Sofsilk Coated Braided Silk Suture Product Description CS-211 SOFSILK* 4-0 BLK 45CM CVF21 X36 CS211 CS-490 SOFSILK* 2-0 BLK 75CM GS11 X36 …

Covidien, LP

FDA Devices Moderate Mar 8, 2023

Finished Goods Box of 50 Inserts and Scanning Labels for Medivac Guardian 3L Catalog Number: FG 12022. Intended adjunct in the estimation of blood …

Stryker Corporation

FDA Devices Moderate Mar 8, 2023

Monosof Monofilament Nylon sutures: Product Description CN-724 MONOSOF* 1 BLK 100CM GS25 X36 CN-791 MONOSOF* 2-0 BLK 100CM GCC90X36 …

Covidien, LP

FDA Devices Moderate Mar 8, 2023

Ultracell Wick with 80cc Collection Bag, 20/box

Beaver Visitec International, Inc.

FDA Devices Moderate Mar 8, 2023

MYLA comprises AST Filters in conjunction with VITEK MS; middleware which connects microbiology laboratory instruments for ID/AST and blood culture …

Biomerieux Inc

FDA Devices Moderate Mar 8, 2023

Surgipro II Monofilament Polypropylene Sutures Product Description Model Number VP-421X SURGIPRO*II 4-0 90CM V20 DA7P VP421X VP-435-X SURGIPRO II …

Covidien, LP

FDA Devices Moderate Mar 8, 2023

Biofinity XR Toric Single Diagnostic lens- Soft (hydrophilic) Contact Lens (extended wear)

CooperVision, Inc.

FDA Devices Critical Mar 8, 2023

Life2000 Ventilator PKG, Hospital, a) REF BT20007, b) REF BT-20-0007, ventilatory support for the care of individuals

Baxter Healthcare Corporation

FDA Devices Moderate Mar 8, 2023

EMPOWR VVC KNEE TIBIAL INSERT, SIZE 6, 22MM, REF: 346-22-706; EMPOWR VVC KNEE TIBIAL INSERT, SIZE 7, 22MM, REF: 346-22-707; EMPOWR VVC KNEE TIBIAL IN…

Encore Medical, LP

FDA Devices Moderate Mar 8, 2023

Phoenix mKDR, digital mobile diagnostic x-ray system

SEDECAL SA

FDA Devices Moderate Mar 8, 2023

Sit to Stand STS500 Patient Lift

Med-Mizer, Inc.

FDA Devices Critical Mar 8, 2023

Life2000 Ventilator System, a) REF BT-20-0002, b) REF BT-20-0002A, ventilatory support for the care of individuals

Baxter Healthcare Corporation

FDA Devices Moderate Mar 8, 2023

Monofilament Nylon Suture (McKesson Branded) and Coated Braided Silk Suture (McKesson Branded) (1) S661GX 5-0 NYLON 18 DS18 (2)S683GX 4-…

Covidien, LP

FDA Devices Moderate Mar 8, 2023

Finished Goods Box of 50 Inserts and Scanning Labels for Medivac Guardian 2L Catalog Number: FG 12010. Intended adjunct in the estimation of blood …

Stryker Corporation

FDA Devices Moderate Mar 8, 2023

stryker Hoffmann LRF, Transport Strut, Model Number 4933-0-400; Orthopedic external fixation device intended to keep bone fragments/segments in a cor…

Stryker GmbH

FDA Devices Moderate Mar 8, 2023

MultiLab Series II REVO non-invasive vascular diagnostic device, Model Number 12950-0000-01

Unetixs Vascular, Inc.

FDA Devices Moderate Mar 8, 2023

Med-Riser MR600 Patient Lift

Med-Mizer, Inc.

FDA Devices Moderate Mar 8, 2023

ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 402S0425, Bone fixation device

Wright Medical Technology, Inc.

FDA Devices Moderate Mar 8, 2023

Novafil Monofilament Polybutester Suture Product Description: 8886 4002-41 NOVAFIL 3-0 BLU 90CM C14 8886 4400-13 NOVAFIL 6-0 BLU 45CM SBE2 8886 …

Covidien, LP

FDA Devices Moderate Mar 8, 2023

MultiLab Series II LHS TI & ERGO non-invasive vascular diagnostic device, Model Number 11949-0000-01

Unetixs Vascular, Inc.

FDA Devices Moderate Mar 8, 2023

CustomEyes kits

Beaver Visitec International, Inc.

FDA Devices Critical Mar 8, 2023

Life2000 Ventilator , REF MS-01-0118, ventilatory support for the care of individuals

Baxter Healthcare Corporation

FDA Devices Moderate Mar 8, 2023

Surgipro Monofilament Polypropylene Sutures Product Description CP-535 SURGIPRO* 1 BLU 100CM GS24 X36 CP-824 SURGIPRO* 1 BLU 150CM GS26 X24 CP-82…

Covidien, LP

NHTSA Critical Mar 8, 2023

FORD 2022-2023: STEERING

FORD

NHTSA Critical Mar 8, 2023

INTERNATIONAL 2023: ELECTRICAL SYSTEM:12V/24V/48V BATTERY

INTERNATIONAL

NHTSA Critical Mar 8, 2023

INTERNATIONAL 2023: POWER TRAIN:DRIVELINE:DRIVESHAFT

INTERNATIONAL

NHTSA Critical Mar 7, 2023

KIA 2021-2023: AIR BAGS:SIDE/WINDOW:CURTAIN

KIA

NHTSA Critical Mar 3, 2023

MACK 2023: STEERING:CRITICAL FASTENERS

MACK

CPSC Moderate Mar 2, 2023

Active Sports Recalls Wakeboard Bindings Due to Fall Hazard (Recall Alert)

CPSC Moderate Mar 2, 2023

DR Power Equipment Recalls PRO XL501 Chipper Shredders Due to Laceration Hazard (Recall Alert)

Generac, of Waukesha, Wisconsin

CPSC Moderate Mar 2, 2023

Helly Hansen Recalls Adult Workwear Sweatshirts and Hoodies Due to Violation of Federal Flammability Standard and Burn Hazard

CPSC Moderate Mar 2, 2023

Multi-Purpose Kids Bike Helmets Recalled Due to Risk of Head Injury; Sold Exclusively on Amazon.com; Sold by Ouwoer Direct (Recall Alert)

Huizhou Lanova Outdoor Product Company, of China

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