cpsc regulated Recalls

2,056 recalls tagged with “cpsc regulated”.

Health & Personal Care

HIGH

FDA DEVICE

Wasatch Photonics Raman Spectrometers Recall Expanded for Laser Safety Risks (2025)

Wasatch Photonics recalled 192 Raman spectrometers in the United States after identifying two potential laser safety failure modes. Models 785-SR-ILP, 785-SR-ILC, 830-SR-ILP, 830-SR-ILC, and 785-ER-ILC are included. The defect could occur under excessive force or extreme continuous vibration. Stop using immediately and follow the manufacturer’s recall instructions.

Aug 4, 2025

WASATCH PHOTONICS

Two new

Health & Personal Care

HIGH

FDA DEVICE

AVID Medical CPT BASIC IR PACK 1646381 Recall for Sterility Risk (2025)

AVID Medical recalls 228 CPT BASIC IR PACKs sold nationwide, including Florida, due to open header bag seals that may compromise sterility. The recall is active as of September 17, 2025. Consumers should stop use and follow manufacturer instructions.

Aug 4, 2025

AVID Medical

Potential for

Health & Personal Care

HIGH

FDA DEVICE

AVID Medical JACK421-04 ENT PACK Recalled for Sterility Risk (2025)

AVID Medical recalled 57 JACK421-04 ENT PACK convenience kits nationwide in Florida. The open header bag seals could compromise sterility. Consumers should stop using the device and follow manufacturer instructions for recall resolution.

Aug 4, 2025

AVID Medical

Potential for

Health & Personal Care

HIGH

FDA DRUG

Hospira Sodium Bicarbonate Vial Recall for Sterility Concerns Affects 15,750 Vials

FDA-listed recall for Hospira brand 8.4% Sodium Bicarbonate Injection affecting 15,750 vials distributed nationwide. The liable lot LH2671, expiring 11/30/2026, is linked to a lack of assurance of sterility. Healthcare providers and patients should stop use and contact Pfizer for guidance.

Aug 4, 2025

Hospira

Lack of

Health & Personal Care

HIGH

FDA DRUG

B. Braun 23,100 0.9% Sodium Chloride Injection Containers Recalled for Sterility Concerns (2025)

B. Braun Medical Inc. recalls 23,100 0.9% Sodium Chloride Injection L 8000 containers nationwide. The recall cites lack of assurance of sterility and potential fluid leakage at a weld site. Stop using immediately and consult a healthcare provider.

Aug 4, 2025

B. Braun Medical Inc.

Lack of

Health & Personal Care

HIGH

FDA DEVICE

Beckman Coulter DxC 500i Clinical Analyzer Modules Recalled for Processing Delays (2025)

Beckman Coulter has issued a recall for 116 DxC 500 AU Module with ISE and DxC 500i components sold internationally. The recall date is 2025-08-04. A processing fault can cause the Clinical Chemistry test to stay In Progress when an Immunoassay test is run between CC tests. Delays may occur. Stop using the device and contact Beckman Coulter for instructions.

Aug 4, 2025

Beckman Coulter

On a

Food & Beverages

HIGH

FDA FOOD

DFA Dairy Brands Frozen Dessert Recalled for Undeclared Wheat and Soy, 324 Containers Affected

DFA Dairy Brands recalls 54 cases (324 containers) of a Friendly's branded frozen dessert due to undeclared wheat and soy. The recall covers product distributed in MD, VA, and PA. Consumers should avoid consumption and contact DFA Dairy Brands for refunds or replacements.

Aug 1, 2025

DFA Dairy Brands

Product contains

Recalled Magnetic Floating Stackers toy, model STA-BGY-801T (Rainbow)

HIGH

CPSC

Tegu Recalls 2 Magnetic Floating Stackers for Magnet Ingestion Hazard (2025)

Tegu recalled two Magnetic Floating Stackers sold at multiple retailers. Models STA-BGY-801T and STA-BTP-806T are affected. The magnets can detach and be ingested, posing a serious injury or death risk. Parents should stop using the toys immediately and contact Tegu for a free replacement.

Jul 31, 2025

Tegu

The recalled

Recalled IKEA 365+ VÄRDEFULL garlic press

MEDIUM

CPSC

IKEA 365+ VARDEFULL Garlic Press Recalled for Laceration and Ingestion Hazards (2025)

IKEA is recalling its 365+ VARDEFULL garlic presses after metal fragments can detach and pose a laceration or ingestion hazard. Consumers should stop using the recalled garlic press immediately and return it to any IKEA store for a full refund. If you cannot return to a store, contact IKEA for disposal instructions to receive the refund.

Jul 31, 2025

IKEA

Small metal

Recalled Amazon Basics Premium Foam Eurotop Mattress

HIGH

CPSC

Amazon Recalls Amazon Basics Premium Foam Eurotop Mattress for Fire Hazard (2025)

Amazon recalled Amazon Basics Premium Foam Eurotop Mattresses sold on Amazon. The nine-inch mattresses in twin, full, queen and king sizes were manufactured from 12/22/2022 through 05/16/2024 and violate the federal flammability standard, posing a fire hazard. Stop using the recalled mattress and contact Amazon for a full refund.

Jul 31, 2025

Amazon

The recalled

Recalled Leatherman Charge Plus (stainless steel)

MEDIUM

CPSC

Leatherman Charge Plus Multi-Tools Recalled for Laceration Hazard — Check Your Model

Leatherman recalled Charge Plus and Charge Plus TTi multi-tools due to a laceration hazard. The knife blade tip does not fully fold into the handle, posing a risk of injuries. Consumers should stop using the tools immediately and check if their multi-tool is affected by visiting the Leatherman website.

Jul 31, 2025

Leatherman

The tip

Recalled Baby Loren Children's Joy Loungewear

HIGH

CPSC

Baby Loren Recalls 4 Morning Loungewear Styles for Burn Risk (2025)

Baby Loren recalls four Morning children’s 100% cotton loungewear dresses in 2025 for fire safety violations. The recall involves dresses with neck labels listing October 2022 or October 2023 and batch numbers ending in 3465, 3585, 3599 or 3569. Consumers should stop using the dresses and contact Baby Loren for a full refund.

Jul 31, 2025

Baby Loren

The recalled

Health & Personal Care

HIGH

FDA DEVICE

Waldemar Link Recall Reaches 8 Units of LinkSymphoKnee Tibial Components Over Uncoated Screws (2025)

Eight modular LinkSymphoKnee TiNbN tibial components are under recall after production with two uncoated security screws. Waldemar Link GmbH & Co. KG disclosed the issue. The devices were distributed worldwide, including CO, IN, NJ and TX in the United States, plus Germany and Italy. Consumers should stop using the device immediately and follow manufacturer instructions.

Jul 31, 2025

Waldemar Link GmbH & Co. KG

Some modular

Health & Personal Care

HIGH

FDA DEVICE

Medline Recalled 7,913 Reprocessed Webster CS Catheters for Electrophysiology Mapping

Medline Industries recalled 7,913 reprocessed Webster CS Catheters for electrophysiology mapping nationwide in the United States. The recall concerns small residual particulates on patient-contacting surfaces that could trigger inflammatory responses or systemic infection. If particulates dislodge and contact circulating blood or the heart, they could cause granulomatous reactions or thrombus, and

Jul 31, 2025

Medline Industries, LP

Specific lots

Health & Personal Care

HIGH

FDA DEVICE

Medline Recalled 7,913 Reprocessed ACUSON AcuNav Ultrasound Catheters for Intracardiac Imaging

Medline Industries recalled 7,913 reprocessed ACUSON AcuNav ultrasound catheters nationwide in the United States. The recall cites residual particulates on patient-contacting surfaces as the hazard. Consumers should stop use and follow manufacturer instructions for recall actions.

Jul 31, 2025

Medline Industries, LP

Specific lots

Health & Personal Care

HIGH

FDA DEVICE

Medline Reprocesses 7,913 Electrophysiology Catheters for Safety Risks

Medline Industries recalled 7,913 reprocessed Inquiry Steerable Diagnostics Catheters due to contamination risks. Some models may contain small residual particulates that can cause severe inflammatory responses or systemic infections. Patients must stop using these devices immediately and contact healthcare providers for further instructions.

Jul 31, 2025

Medline Industries, LP

Specific lots

Health & Personal Care

HIGH

FDA DEVICE

Medline Livewire Steerable EP Catheters Recalled for Particulates in 2025 (7,913 Units)

Medline recalled 7,913 reprocessed Livewire steerable electrophysiology catheters distributed nationwide in the United States. The devices may contain small residual particulates on patient-contacting surfaces, potentially triggering an inflammatory response or systemic infection. Stop using the device and follow recall instructions from Medline or your healthcare provider.

Jul 31, 2025

Medline Industries, LP

Specific lots

Health & Personal Care

HIGH

FDA DEVICE

Fortress Introducer Sheath System 386594 Recall Expanded; 2,500 Units Worldwide Distribution (High-R

Fortress Introducer Sheath System recalled 2,500 units linked to label mispackaging. The devices were distributed worldwide, including 15 U.S. states and numerous international markets. The incorrect pouch label lists the 4F version reference and unique device identifier instead of the packaged 6F version. Healthcare providers must stop use and follow manufacturer recall instructions.

Jul 30, 2025

Fortress Introducer Sheath System

Units may

Health & Personal Care

HIGH

FDA DRUG

Exela Pharma Sciences 4.2% Sodium Bicarbonate Injection Recalled Over Arsenic Impurity Out-Of-Spec

Exela Pharma Sciences recalls 4.2% Sodium Bicarbonate Injection, USP, 5 mEq/10 mL, nationwide in the U.S. The recall cites out-of-spec arsenic impurities. Consumers should stop use and contact a healthcare provider. Follow recall notice for guidance and refunds.

Jul 30, 2025

SODIUM BICARBONATE

Failed Impurities/Degradation

Health & Personal Care

HIGH

FDA DRUG

Pfizer Levoxyl Recall: Subpotent Levoxyl 50 mcg Tablets, 29,004 Bottles in U.S. Market (2025)

Pfizer's Levoxyl 50 mcg levothyroxine tablets are recalled due to subpotency. About 29,004 bottles distributed in the U.S. since distribution. Consumers should stop use and contact their healthcare provider for guidance.

Jul 29, 2025

Levoxyl

Subpotent drug

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Tag Statistics

Total Recalls

2,056

cpsc regulated Recalls

Tag Statistics

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