immediate action Recalls

2,756 recalls tagged with “immediate action”.

Health & Personal Care
HIGH
FDA DEVICE

Tandem Diabetes Care Insulin Infusion Pumps Recalled 1,380 Units in 2026 Over Czech Guide Error

Tandem Diabetes Care recalled 1,380 insulin infusion pumps distributed internationally in the Czech Republic and Slovakia after translation errors in the Czech user guide could cause unintended insulin delivery. The most significant error told users to verify the infusion set is connected to the body when it should be confirming it is not connected. Following this instruction could result in a hyp

Tandem Diabetes Care
The Czech
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Health & Personal Care
HIGH
FDA DEVICE

Medtronic MiniMed 780G Recall 2026: 26,851 Pumps Hit Over Software Defects

Medtronic MiniMed recalled 26,851 MiniMed 780G insulin pumps sold worldwide, including the United States and Israel. Three software defects tied to updates 6.60, 6.61, and 6.62 could misdose insulin. Stop using the affected pumps and follow the recall letter for instructions.

Medtronic MiniMed
Three software
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Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter AU5800 Chemistry Analyzer Recall for 47 Units Over Calibration Delay Issues (2026)

Beckman Coulter Mishima K.K. recalled 47 AU5800 chemistry analyzers sold nationwide in the United States after a software delay can cause calibration and reagent databases to fail to open. The issue occurs when a calibration monitor using Microsoft SQL Server 2022 Express remains open for more than 15 minutes, potentially halting analysis. Healthcare facilities should stop using the devices and (a

Beckman Coulter
A delay
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Health & Personal Care
HIGH
FDA DEVICE

Medline Chest Drainage Units Recall Updated IFUs for Adults 18+

Medline Industries recalls 2,894 Aqua-Seal Chest Drainage Units from Cardinal Health after updating IFUs to specify adult patients 18 years and older. The devices were distributed worldwide, including California, Chile and Panama. The update clarifies intended patient population and requires action from healthcare providers to stop use until further notice.

Medline Industries, LP
The instructions
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Food & Beverages
HIGH
FDA FOOD

Reser's Tuna Salad Recalled Over Undeclared Fish Allergen

Reser's Fine Foods recalled 298 tubs of Tuna Salad on January 30, 2026 due to undeclared fish allergens. The product was mislabeled with a Chicken Salad lid, posing a risk to consumers with fish allergies. The recall affects distribution in Arizona, California, Nevada, Utah, and Washington.

Reser's Fine Foods
Undeclared fish
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Health & Personal Care
HIGH
FDA DEVICE

ReCor Medical Paradise Ultrasound Renal Denervation System Recall 2026: 24 Catheters PRDS-068-02

ReCor Medical Inc. has issued an active recall for 24 Paradise ultrasound renal denervation catheters distributed nationwide in nine states. The devices were nonconforming and were supposed to be scrapped and not for human use. Healthcare providers and patients should stop using the devices immediately and await manufacturer recall instructions.

ReCor Medical
Due to
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Health & Personal Care
HIGH
FDA DEVICE

Paradise Renal Denervation Catheter Recalled for 1 Unit in 2026

Paradise Renal Denervation Catheter was recalled after a single unit distributed nationwide in nine states was deemed nonconforming and not for human use. The device is an ultrasound renal denervation catheter. Healthcare providers should stop using it and contact ReCor Medical for instructions.

Paradise
Due to
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Recalled Teether Toy – Red
HIGH
CPSC

AiTuiTui Pull String Teething Toys Recalled for Choking Hazard

AiTuiTui recalled its Pull String Teething Toys on January 29, 2026, due to a choking risk. The toys do not meet mandatory safety standards, posing a potential risk of serious injury or death. Consumers should stop using the teething toys immediately and contact the manufacturer for a refund.

AiTuiTui Pull String Teething Toys
The hair
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Recalled Sunneday Oasis Cottage Above-Ground Pool Models 70018 and 70024
MEDIUM
CPSC

Hobby Lobby Recalls Above-Ground Pools Due to Drowning Hazard

Hobby Lobby recalled above-ground pools manufactured by Starmatrix Group on January 29, 2026. The pools pose a drowning risk due to a design flaw that creates a foothold for children. Consumers should stop using these pools immediately and contact Starmatrix for a free repair kit.

Starmatrix Group Inc., of China
The compression
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Health & Personal Care
HIGH
FDA DEVICE

Olympus MAJ-210 Single-Use Biopsy Valve Recalled for 95,882 Boxes Nationwide (2026)

Olympus Corporation of the Americas recalls 95,882 boxes of MAJ-210 single-use biopsy valves distributed nationwide to hospitals and clinics in the United States after reports of rubber fragments detaching during use. The defect can release fragments into the endoscope channel or patient. Healthcare facilities should stop using the device immediately and follow recall instructions.

Olympus
Potential for
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Health & Personal Care
HIGH
FDA DRUG

Teva Metoprolol Succinate 200 mg Recall Affects 19,056 Bottles Nationwide (2026)

Teva Pharmaceuticals recalled 19,056 bottles of Metoprolol Succinate Extended-Release Tablets, 200 mg, sold nationwide. The recall cites failed dissolution specifications, which could affect how the drug releases in the body. Patients should stop using the product and contact Teva or their healthcare provider for guidance.

METOPROLOL SUCCINATE
Failed Dissolution
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Health & Personal Care
HIGH
FDA DRUG

Teva Metoprolol Succinate 25 mg Recall for 18,780 Bottles Nationwide in 2026

Teva Pharmaceuticals is recalling 18,780 bottles of Metoprolol Succinate Extended-Release Tablets, 25 mg, distributed nationwide. The recall is due to failed dissolution specifications that could affect dosing. Patients should stop using affected bottles and contact Teva or their healthcare provider for guidance.

Metoprolol Succinate
Failed Dissolution
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Recalled Bazic Silicone Glue – Front and Side
HIGH
CPSC

Bazic Products Recalls Silicone Glue Over Child Poisoning Risk

Bazic Products recalled Bazic Silicone Glue on January 29, 2026, due to a serious poisoning risk for children. The glue's packaging does not meet child-resistant standards, violating federal law. Consumers should stop using the product immediately and seek a full refund.

Bazic Products
The glue
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Violative LuxJet Submersible LED Lights
HIGH
CPSC

LuxJet LED Lights Recalled Due to Battery Ingestion Risk

LuxJet recalled Submersible LED Lights on January 29, 2026, due to ingestion risks from lithium batteries. The recall affects sets of 10 lights sold with multiple batteries. Consumers must stop using the lights and return them for a refund.

LuxJet Submersible LED Lights
The recalled
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Recalled Mindbodygreen Ultimate Multivitamin+ Dietary Supplement Bottle
HIGH
CPSC

Mindbodygreen Recalls Multivitamin Due to Child Poisoning Risk

Mindbodygreen recalled Ultimate Multivitamin+ dietary supplements on January 29, 2026, due to a risk of child poisoning. The bottles lack child-resistant packaging, violating safety standards. Consumers should stop using the product immediately and secure it out of children's reach.

Arizona Nutritional Supplements, of Chandler, Arizona
The bottles
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Tag Statistics

Total Recalls
2,756

Related Tags

electrical hazardbattery poweredlithium batterystop use immediatelyreturn for refundreplacement availablefda regulatedcpsc regulatedinfant productadult productelderly productmetal