immediate action Recalls

2,679 recalls tagged with “immediate action”.

Recalled Built LUUM LED Tumbler - FESTIVE FOREST
HIGH
CPSC

Lifetime Brands Recalls BUILT LUUM Light Up Tumblers for Choking and Battery Ingestion Hazards (2026

Lifetime Brands recalls BUILT LUUM Light Up Tumblers sold at multiple retailers. The recall covers 16 oz and 18 oz plastic cups with a lid and straw that contain a bottom LED light powered by a button cell battery. Labels on the underside or hangtags show the theme and item numbers with UPCs. Stop using these tumblers immediately and seek a full refund by contacting Lifetime Brands.

Lifetime Brands
The recalled
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Health & Personal Care
MEDIUM
FDA DRUG

AvKARE Recalls Rosuvastatin Tablets Due to Dissolution Issues

AvKARE recalled 7,991 cartons of Rosuvastatin Tablets on December 31, 2025. The recall stems from the product being out of specification for dissolution. Consumers should stop using the medication immediately and consult healthcare providers for guidance.

MAGNESIUM SULFATE
Product mix
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Health & Personal Care
HIGH
FDA DRUG

Teva Octreotide Acetate Injectable Suspension Recall 21,930 Cartons Over Sterility Risk (2026)

Teva Pharmaceuticals recalled 21,930 cartons of Octreotide Acetate for Injectable Suspension distributed nationwide in the United States. The recall stems from lack of assurance of sterility identified during an FDA inspection at the contract manufacturer. Healthcare providers and patients should stop using this product immediately and contact Teva or a physician for guidance.

OCTREOTIDE ACETATE
Lack of
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Health & Personal Care
HIGH
FDA DEVICE

Straumann USA Recalls 13 Custom Abutment Ti RC for TAN Material Mix-Up (2026)

Straumann USA recalled 13 Custom Abutment Ti RC units distributed worldwide, including the United States and Canada. A TAN material was misidentified as Titanium Ti Gr4 D during manufacturing, causing RC Titanium abutments to be made from TAN material. Clinics and patients should stop using the devices immediately and follow recall instructions from Straumann USA or their healthcare providers.

Straumann USA
A material
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Health & Personal Care
HIGH
FDA DEVICE

Straumann USA Recalls 7 Custom Abutment AS Ti for Straumann RC Over TAN Material (2026)

Straumann USA LLC recalls 7 Custom Abutment AS Ti for Straumann RC. The recall follows a material mix-up during manufacturing. A TAN material bar was incorrectly identified as Titanium Bar Ti Gr4 D, causing RC Titanium abutments to be made with TAN material. Stop using the device and contact Straumann for instructions immediately.

Straumann USA
A material
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Health & Personal Care
HIGH
FDA DRUG

Teva Octreotide Acetate Injectable Suspension Recall 19,869 Cartons Nationwide (2026)

Teva Pharmaceuticals USA recalled 19,869 cartons of Octreotide Acetate for Injectable Suspension nationwide in the United States after FDA inspection flagged lack of assurance of sterility at the contract manufacturer. The FDA cited quality system deficiencies at Pharmathen International S.A. in Greece. Healthcare providers and patients should stop using the product immediately and contact Teva or

OCTREOTIDE ACETATE
Lack of
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Health & Personal Care
HIGH
FDA DRUG

Teva Octreotide Acetate Injectable Suspension Recall Expanded in 2026 for Sterility Concerns

Teva Pharmaceuticals recalled 1,897 cartons of Octreotide Acetate for Injectable Suspension distributed nationwide in the USA after an FDA inspection flagged sterility concerns. The recall is due to lack of assurance of sterility from the contract manufacturer. Consumers and healthcare providers should stop using the product immediately and contact Teva for guidance.

OCTREOTIDE ACETATE
Lack of
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Food & Beverages
HIGH
FDA FOOD

POCAS INTERNATIONAL Recalls 425 Cases of POPPING BOBA Strawberry Dragon F/OOLONG Tea (2026)

POCAS INTERNATIONAL recalled 425 cases of POPPING BOBA RTD Strawberry Dragon F/OOLONG Tea distributed in NY, VA, FL, MA, TX, LA, UT, CA and Canada. The recall cites a packaging integrity issue that may compromise product quality. Consumers should not consume the product and should contact Pocas International by email for refunds or replacements.

Pocas International
Packaging integrity
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Food & Beverages
HIGH
FDA FOOD

Lucerne 2% Cottage Cheese 24 oz Recalled for Metal Fragments in 2026 Recall

Lucerne recalled 12,222 tubs of 2% cottage cheese sold at Albertsons stores after metal fragments were found in packaging. The object is a curled stainless steel spring and could end up in the product. Stop using the product and contact Albertsons Companies LLC for a refund or replacement.

Albertsons Companies
Metal fragments.
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Food & Beverages
HIGH
FDA FOOD

Pocas International Recalls Popping Boba Peach Oolong RTD Tea 12x13.8oz (2026)

Pocas International recalled 370 cases of Popping Boba RTD Peach Oolong Tea sold in NY, VA, FL, MA, TX, LA, UT, CA and Canada. A packaging integrity issue may compromise product quality. Consumers should not consume the product and should contact Pocas International Corp. for refund or replacement via email.

Pocas International
Packaging integrity
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Food & Beverages
HIGH
FDA FOOD

POCAS International Recalls Popping Boba RTD Mango Passion Fruit Green Tea 12 x 13.8 oz (2026)

Pocas International recalled 517 cases of Popping Boba RTD Mango Passion Fruit Green Tea distributed to NY, VA, FL, MA, TX, LA, UT, CA and Canada. A packaging integrity issue may compromise product quality. Consumers who purchased it should not consume the beverage and should contact Pocas International for refund or replacement via email.

Pocas International
Packaging integrity
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Food & Beverages
HIGH
FDA FOOD

Pocas International Recalls POPPING BOBA RTD Mixed Berry Hibiscus Tea (12 x 13.8 oz) 2026

Pocas International Corp. recalls 148 cases of POPPING BOBA RTD Mixed Berry Hibiscus Tea distributed to New York, Virginia, Florida, Massachusetts, Texas, Louisiana, Utah, California and Canada. A packaging integrity issue may compromise product quality. Consumers who purchased should not consume it and should contact Pocas International for refund or replacement information via email.

Pocas International
Packaging integrity
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Food & Beverages
HIGH
FDA FOOD

Western Mixers Produce & Nuts Recalls 1 Case Treasured Harvest Chilli Spanish Peanuts (2026)

One case of Treasured Harvest Chilli Spanish Peanuts, 25 lb bags, from Western Mixers Produce & Nuts was recalled after a glass fragment was found inside a sealed bag. The recall covers two consignees with 53 retail locations nationwide. Consumers should not consume this product and should contact the company for a refund or replacement via email.

Western Mixers Produce & Nuts
Foreign object
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Recalled 17 Stories Furniture 14-Drawer Dresser (front)
HIGH
CPSC

17 Stories Furniture Dressers Recalled Over Tip-Over Risk

17 Stories Furniture recalled its 14-drawer dressers on March 12, 2026, due to serious tip-over hazards. The dressers, sold in black, white, and brown, can pose risks of injury or death to children if not anchored. Model numbers include 55SCDR14KDBRDL and 55SCDR14KDCHDL.

Online at Wayfair.com from September 2023 through January 2026 for about $135.
The recalled
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Recalled LIVEHOM 11-Drawer Dresser – brown
HIGH
CPSC

LIVEHOM Dressers Recalled Over Tip-Over Hazard Risk

LIVEHOM recalled 11-Drawer Dressers on March 12, 2026, due to tip-over hazards. The recall affects dressers sold on Amazon that can pose serious risks to children. Consumers must stop using these dressers immediately and contact the company for a full refund.

LIVEHOM 11-Drawer Dressers
The recalled
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Tag Statistics

Total Recalls
2,679

Related Tags

choking hazardbattery poweredlithium batteryinfant productchildren productkitchenstop use immediatelyreturn for refundreplacement availablechemical hazardadult productcpsc regulated