stop use immediately Recalls

2,228 recalls tagged with “stop use immediately”.

Health & Personal Care
HIGH
FDA DRUG

Macleods Pharma USA Recalls 1,315 Levothyroxine 150 mcg Tablets (2026)

Macleods Pharma USA, Inc. recalls 1,315 bottles of Levothyroxine Sodium Tablets USP 150 mcg distributed nationwide. The drug is subpotent, which may not provide the full therapeutic dose. Stop using and contact your healthcare provider or Macleods Pharma USA, Inc. for guidance.

LEVOTHYROXINE SODIUM
Subpotent Drug
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Food & Beverages
HIGH
FDA FOOD

American Laboratories Pepsin Powder Recall 468 kg Over Salmonella Contamination (2026)

American Laboratories recalled 468 kg of Pepsin 1:3000 Powder distributed through 11 wholesale accounts in the United States and one in Australia. The powder is potentially contaminated with Salmonella and could cause illness if used. Consumers who purchased this product should not consume it and should contact American Laboratories by email for refund or replacement.

American Laboratories
Potential Salmonella
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Food & Beverages
HIGH
FDA FOOD

American Laboratories Recalls 370 kg Pepsin 1:10,000 Powder Over Salmonella Risk (2026)

American Laboratories recalled 370 kg of Pepsin 1:10,000 Powder sold through 11 wholesale accounts in AZ, CA, FL, MO, NM, OH, SC, UT, WI and one account in Australia after a potential Salmonella contamination. The product carries a possible Salmonella contamination risk. Consumers should not consume the product and should contact American Laboratories for refund or replacement via email.

American Laboratories
Potential Salmonella
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Food & Beverages
HIGH
FDA FOOD

American Laboratories Pepsin Full Strength Powder Recalled for Salmonella Contamination (400 kg, 202

American Laboratories recalled 400 kg of Pepsin Full Strength Powder sold to 11 direct wholesale accounts in AZ, CA, FL, MO, NM, OH, SC, UT, WI and one wholesale account in Australia after a recall cited potential Salmonella contamination. The product is Item #5000545 and packed in double poly-lined drums or boxes. Consumers should not consume this product and should contact American Laboratories,

American Laboratories
Potential Salmonella
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Recalled TheKiddoSpace LED Soccer Hover Ball
HIGH
CPSC

TheKiddoSpace Recalls LED Soccer Hover Balls Over Burn Risk

TheKiddoSpace recalled LED soccer hover balls on February 26, 2026, due to a burn hazard. The balls exceed the allowable surface temperature for batteries, posing serious injury risks. Consumers should stop using these toys immediately and seek a replacement.

TheKiddoSpace
The surface
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Recalled Dupray Neat Steam Cleaner
HIGH
CPSC

Dupray Recalls Neat Steam Cleaners Over Burn Hazard Risk

Dupray USA recalled portable Neat Steam Cleaners on February 26, 2026, due to burn hazards. The model number is DUP020WNA, with batch codes from 0118-01 to 0425-05. Consumers should stop using the product immediately and follow safety instructions for a free replacement part.

Dupray USA
The steam
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Recalled High Bay Linear LED light fixture
HIGH
CPSC

PQL Recalls High Bay Linear LED Light Fixtures Due to Fire Hazard

PQL recalled High Bay Linear LED light fixtures on February 26, 2026, due to a fire hazard. The retaining pins securing the LED board can degrade, causing the board to come loose. Consumers should stop using the fixtures and contact PQL for free replacement parts.

Jiangsu Ever-Tie Lighting Co., Ltd, of China
The retaining
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Recalled Royal Oak Flame Saber Lighter
HIGH
CPSC

Royal Oak Recalls Lighters Over Serious Fire and Burn Hazards

Royal Oak Enterprises recalled flame saber lighters on February 26, 2026, due to serious fire and burn hazards. The lighters lack child-resistant mechanisms and violate labeling requirements. Consumers should stop using these lighters immediately and seek a refund.

Royal Oak Enterprises
The recalled
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Recalled TheKiddoSpace Sensory Story Book
HIGH
CPSC

TheKiddoSpace Recalls Children's Story Books Over Choking Hazard

TheKiddoSpace recalled children's story books on February 26, 2026, due to a choking hazard. The felt parts of the books may detach, posing a risk to children. Consumers should stop using the books immediately and contact TheKiddoSpace for a full refund.

TheKiddoSpace
The recalled
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Recalled TheKiddoSpace Toy - Peg Dolls in Cups
HIGH
CPSC

TheKiddoSpace Recalls Peg Doll Toys Due to Choking Hazard

TheKiddoSpace recalled peg doll toys on February 26, 2026, due to a choking hazard. The toys can block a child's airway, posing a risk of serious injury or death. Consumers should stop using the toys immediately and return them for a full refund.

TheKiddoSpace
The recalled
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Recalled Somgem Lightweight Tiny Pinky Pig Lighter
HIGH
CPSC

Somgem and Yomin Toilet Lighters Recalled for Fire Hazard

Somgem and Yomin recalled pig and toilet lighters on February 26, 2026. The lighters lack child-resistant features, posing serious burn risks. Consumers should stop using these products immediately and seek refunds.

Somgem Pig and Yomin Toilet Lighters
The recalled
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Recalled SumDirect LED Mini Blinking Lights
HIGH
CPSC

SumDirect LED Mini Lights Recalled Over Battery Ingestion Risk

SumDirect recalled LED mini lights on February 26, 2026, due to a serious ingestion risk from button cell batteries. The recall affects products that are easily accessible to children and lack required safety warnings. Consumers should stop using the lights immediately and seek a refund.

SumDirect LED Mini Lights
The recalled
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Recalled Babysense Max View 5.5" Baby Monitor display/parent unit
HIGH
CPSC

Babysense Max View Baby Monitors Recalled Due to Fire Hazard

Hisense recalled Babysense Max View baby monitors on February 26 after reports of overheating display units. The recall affects model VBM55, with incidents of sparking during charging. Consumers should stop using the device immediately and contact Hisense for a replacement.

Hisense Ltd., of Israel
The display
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Health & Personal Care
HIGH
FDA DEVICE

Synthes Bone Taps Recall 33-Unit Lot Swap Causes Incorrect Threading (2026)

Synthes bone taps recalled nationwide in the United States after a lot swap affected 33 units sold through multiple retailers. The defect is an incorrect thread caused by a lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8. Healthcare providers should stop using these devices immediately and follow recall instructions from Synthes.

Synthes
A full
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Recall: 93 PKS Cutting Forceps Over Welding Defects (2026)

Olympus Corporation of the Americas recalled 93 PKS Cutting Forceps worldwide due to welding defects that can cause the jaw to break during clinical use. The issue involves Model 3005PK and UDI 00821925036000. Action is required immediately and providers should follow recall instructions.

Olympus Corporation of the Americas
Olympus identified
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    stop use immediately Recalls | RecallRadar