glass Recalls

160 recalls tagged with “glass”.

Recalled Séfralls Minoxidil Hair Generation Serum
CRITICAL
CPSC

Séfralls Minoxidil Hair Generation Serum Recalled for Child Poisoning Risk (2025)

Séfralls Minoxidil Hair Generation Serum, sold by Guangzhou Ariel Biotech, was recalled on August 7, 2025. The serum is packaged in amber dropper bottles with a white and gold dropper and a white, black and gold label. The packaging is not child-resistant, violating the Poison Prevention Packaging Act and creating a poisoning risk for children. Consumers should stop using the serum immediately and

Séfralls
The hair
Read more
Food & Beverages
HIGH
FDA FOOD

Hi-Tech Pharmaceuticals’ PrimeNutrition PhytoForm Fruits & Greens Recall for Unapproved Drug Claims

Hi-Tech Pharmaceuticals recalled 85,950 units of PrimeNutrition PhytoForm Fruits & Greens Formula after FDA enforcement flagged unapproved drug claims and misbranding. The dietary supplement was distributed to 40+ states before the recall was issued on 2025-08-06 and remains active. Consumers should not consume the product and should seek refund or replacement from Hi-Tech Pharmaceuticals.

Hi-Tech Pharmaceuticals
Unapproved Drug
Read more
Health & Personal Care
HIGH
FDA FOOD

Hi-Tech Pharmaceuticals Formutech Nutrition Joint Formula Recalled for Unapproved Drug Claims (2025)

Hi-Tech Pharmaceuticals recalled 85,950 units of Formutech Nutrition Flexible Joint Formula with Cissus Quadrangularis sold nationwide after regulators flagged unapproved drug claims. The product claims to support tendons and muscles and promote healthy cartilage, which regulators say is not approved. Consumers who purchased the supplement should not use it and should await refund or replacement,'

Hi-Tech Pharmaceuticals
Unapproved Drug
Read more
Food & Beverages
HIGH
FDA FOOD

Hans Kissle Company Recalls 66 Units of Red Bliss Potato Salad for Undeclared Wheat (2025)

Hans Kissle Company recalled 66 units of Red Bliss Potato Salad distributed in MA, RI, CT, NJ and NY. The recall is due to undeclared wheat and a mislabeling that identifies the product as potato salad while the unit contains pasta salad. Consumers should not eat the product and should contact Hans Kissle Company for refund or replacement via email.

Hans Kissle Company
Contains undeclared
Read more
Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter DxC 500i Clinical Analyzer Modules Recalled for Processing Delays (2025)

Beckman Coulter has issued a recall for 116 DxC 500 AU Module with ISE and DxC 500i components sold internationally. The recall date is 2025-08-04. A processing fault can cause the Clinical Chemistry test to stay In Progress when an Immunoassay test is run between CC tests. Delays may occur. Stop using the device and contact Beckman Coulter for instructions.

Beckman Coulter
On a
Read more
Health & Personal Care
HIGH
FDA DEVICE

BioFire Defense FilmArray NGDS Warrior Panel NGDS-ASY-0007 Recall 130 Kits in 2025

BioFire Defense recalled 130 FilmArray NGDS Warrior Panel NGDS-ASY-0007 kits distributed nationwide in the United States. The recall cites an increased risk of internal control failures when testing positive blood cultures. Clinicians should stop using the device immediately and follow recall instructions provided by BioFire Defense. Notification is by letter to affected facilities.

BioFire Defense
FilmArray NGDS
Read more
Vehicles & Parts
HIGH
NHTSA

Honda 2025 CR-V Hybrid Recall for Fuel Hose Installation Could Cause Fire (TLS)

Honda recalls 2025 CR-V Hybrid vehicles sold through Honda dealers nationwide after finding an improperly installed fuel feed hose that may leak. The recall is identified by Honda as TLS. Dealers will replace the fuel feed hose and install a new connector cover at no charge. Owners should contact Honda at 1-888-234-2138 for service.

Honda
A fuel
Read more
Health & Personal Care
HIGH
FDA DEVICE

bioMerieux VITEK 2 AST Cards Recalled for False Colistin Results (235,269 Cards) 2025

bioMerieux recalled 235,269 VITEK 2 Gram-negative AST test cards containing Colistin cs02n, distributed internationally. The cards may produce false resistant results for Colistin when testing certain multi-drug-resistant bacteria. Healthcare providers should stop using the affected cards immediately and follow the recall instructions from bioMerieux.

bioMerieux
Potential for
Read more
Health & Personal Care
HIGH
FDA DEVICE

Orthofix Pillar SA Ti Spinal Implant Recalled for Labeling Error (2025)

Orthofix U.S. recalled 3 Pillar SA Ti intervertebral body fusion devices nationwide in the United States after a labeling discrepancy. The 37 mm implant width is correct on the front label, but the outer side flap and inner label information box incorrectly state 33 mm. Healthcare providers and patients should stop using the device immediately and await manufacturer instructions.

Orthofix U.S.
A 37
Read more
Health & Personal Care
HIGH
FDA DEVICE

Sedecal MobileDiagnost wDR 2.2 Recall for 1,198 Units in 2025

Sedecal recalled 1,198 MobileDiagnost wDR 2.2 mobile X-ray systems distributed in California, Illinois and New Jersey. The company reminded users the equipment is not water-resistant and must be cleaned strictly according to the manual. Improper cleaning could have consequences outlined by Sedecal. Health care providers should stop using the device immediately and follow recall instructions.

Sedecal
Sedecal sent
Read more
Health & Personal Care
HIGH
FDA DEVICE

Sedecal SA SM-40HF-B-D-C Mobile X-ray System Recalled for 27 Units in 2025

Sedecal SA recalled 27 SM-40HF-B-D-C mobile X-ray systems distributed in California, Illinois and New Jersey after warning consignees the equipment is not water-resistant and must be cleaned per the manual. The notice outlines possible consequences of improper cleaning. Hospitals and providers should stop using the device immediately and follow recall instructions.

Sedecal SA
Sedecal sent
Read more
Vehicles & Parts
HIGH
NHTSA

Mercedes-Benz GLE 450E 4MATIC Recall for Rearview Mirror Attachment (2025)

Mercedes-Benz USA is recalling certain 2024 GLE 350 4MATIC, 2025 GLE 450e 4MATIC, and additional models sold through its dealer network. The issue involves a multi-purpose camera and rearview mirror that may detach from the windshield. Dealers will replace the windshield and reinstall the camera and mirror at no charge.

Mercedes-Benz
A detached
Read more
Food & Beverages
HIGH
FDA FOOD

PRIMO NO. 1 IN PRODUCE Recalled 89 Boxes of Sliced Cucumber for Salmonella Contamination (2025)

PRIMO NO. 1 IN PRODUCE recalled 89 boxes of sliced cucumber packaged in 2/10-lb boxes distributed to Virginia, New York, Pennsylvania and New Jersey after Salmonella contamination. The recall is active and classified as high risk. Consumers should not eat the product and should contact PRIMO NO. 1 IN PRODUCE for refund or replacement.

PRIMO NO. 1 IN PRODUCE
Product contaminated
Read more
Previous
12345...8

Tag Statistics

Total Recalls
160

Related Tags

chemical hazardpoisoning riskchildren productcpsc regulatedimmediate actionreplacement availableplasticadult productreturn for refundsuffocation riskfda regulatedworkplace
    glass Recalls | RecallRadar