
stop use immediately Recalls
2,229 recalls tagged with “stop use immediately”.

Clonidine Transdermal System Recall Expanded for CGMP Deviations in 113,943 Cartons (2026)
Teva-affiliated Clonidine Transdermal System recalls 113,943 cartons after CGMP deviations. Unapproved raw material prompts recall. Stop use immediately and contact Teva or a healthcare provider for guidance.
Riverence Smoked Trout Dip Recall for Milk Allergen Labeling Error (High)
Label declares cream cheese but does not declare milk
Teva Clonidine Transdermal System Recall Expands Over CGMP Deviations, 124,054 Cartons Affected (202
CGMP Deviations: use of an unapproved raw material

Wagner Spray Tech Recalls 900-Series Power Steamers Over Burn Hazard (2026)


Electrolux Group Recalls Frigidaire Gas Ranges for Burn Hazard (2026)

Specialized Recalls 2026 Turbo Como SL Electric Bicycles Over Fork Fatigue Crack Fall Hazard

Amazon Basics Camping Folding Pocket Knife Recalled for Laceration Hazard (2026)
Amazon recalled the Amazon Basics Camping Folding Pocket Knife sold by Amazon after a laceration hazard was identified. The knife has a 3.5-inch blade. The folding mechanism can fail to remain securely closed, posing a risk of serious cuts.

Lifetime Brands Recalls BUILT LUUM Light Up Tumblers for Choking and Battery Ingestion Hazards (2026
Teva Octreotide Acetate Injectable Suspension Recall 21,930 Cartons Over Sterility Risk (2026)
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
Curosurf 240 mg Poractant Alfa Recalled for Sterility Concerns (2026)
Chiesi USA recalled 7,235 Curosurf vials distributed nationwide to hospitals and clinics. The recall cites a lack of assurance of sterility. Healthcare providers should stop using the product immediately and contact Chiesi USA for guidance.
Straumann USA Recalls 13 Custom Abutment Ti RC for TAN Material Mix-Up (2026)
Straumann USA Recalls 7 Custom Abutment AS Ti for Straumann RC Over TAN Material (2026)
Teva Octreotide Acetate Injectable Suspension Recall 19,869 Cartons Nationwide (2026)
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
Teva Octreotide Acetate Injectable Suspension Recall Expanded in 2026 for Sterility Concerns
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
Xanax XR Alprazolam Recall Over Failed Dissolution Specifications Affects US Nationwide Distribution
POCAS INTERNATIONAL Recalls 425 Cases of POPPING BOBA Strawberry Dragon F/OOLONG Tea (2026)
Packaging integrity issue that may compromise product quality .
Lucerne 2% Cottage Cheese 24 oz Recalled for Metal Fragments in 2026 Recall
Metal fragments. The potential foreign object is a hard, metal (stainless steel), curled spring. Dimensions of a similar spring measure 2.27mm in cross-sectional thickness and 25.38mm in coil width. Spring ends are not sharp but may be sharp if broken/ cut.