stop use immediately Recalls

1,862 recalls tagged with “stop use immediately”.

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
Read more
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
Read more
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
Read more
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
Read more
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
Read more
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
Read more
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.
Read more
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
Read more
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
Read more
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
Read more
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
Read more
Food & Beverages
HIGH
FDA FOOD

Lone Star Dairy Products Recalls 1.79M Lbs Spray Dried Dairy Powder Over Salmonella Risk (2026)

Lone Star Dairy Products LLC issued an active recall of 1.79 million pounds of spray dried dairy powder sold in the United States after Salmonella spp. was identified in finished product testing. The affected product is packaged in 25 kg bags or 1 metric ton totes. Consumers should not consume the product and should contact Lone Star Dairy Products LLC for refund or replacement information via e‑m

Lone Star Dairy Products
Salmonella spp.
Read more
Food & Beverages
HIGH
FDA FOOD

Nuts.com Espresso Malted Milk Balls Recalled for Undeclared Wheat and Soy (2026)

Nuts.com recalled 10,190 pounds of Espresso Malted Milk Balls distributed nationwide in the United States. The recall cites undeclared wheat and soy allergens from soy lecithin in the ingredient statement. Consumers who bought this product should not consume it and should contact Nuts.com for a refund or replacement via email.

Nuts.com
Undeclared Allergen
Read more
Vehicles & Parts
HIGH
NHTSA

Volkswagen Recalls 2025 ID. BUZZ Over Seat Belt Issue

Volkswagen recalls 2025 ID. BUZZ vehicles due to a seating design flaw. The third-row seat accommodates three passengers but only provides two seat belts. This design fails to meet federal safety standards for occupant crash protection.

Volkswagen
In the
Read more
Previous
12345...94
Next

Tag Statistics

Total Recalls
1,862

Related Tags

fire hazardburn riskchemical hazardinfant producttoddler productadult productelderly productimmediate actionreturn for refundfda regulatedcpsc regulatednhtsa regulated