adult product Recalls

915 recalls tagged with “adult product”.

Health & Personal Care
HIGH
FDA DEVICE

Medline Excelsior Medical 0.9% Saline Flush Syringes Recalled Over Concentration Deviation (8.27M)

Medline Recall: Excelsior Medical 0.9% Sodium Chloride Injection, USP, 10 mL fill prefilled saline flush syringes EMZ111240 is being recalled. The notice covers 8,267,150 syringes distributed across the United States and Canada. The risk is a concentration deviation of sodium chloride. Healthcare facilities should stop using the product and follow recall instructions. See the FDA recall page for完整

Medline Industries, LP
Medline has
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Health & Personal Care
HIGH
FDA DEVICE

Olympus BF-XT190 Bronchovideoscope Recall for IFU Updates Over Laser and HF Therapy Use

Olympus Corporation of the Americas recalls 361 units in the US and 258 units overseas as of September 11, 2025. The recall targets the EVIS EXERA b Bronchovideoscope BF-XT190. The update adds safety instructions for using bronchoscopes with laser, argon plasma coagulation, and high-frequency therapy equipment. Patients and healthcare providers should stop using the device immediately and follow a

Olympus Corporation of the Americas
Additional IFU
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Food & Beverages
HIGH
FDA FOOD

Gina Marie Bakery Biscotti Recalled for Undeclared Red 40

Gina Marie Bakery LLC recalled 172 cases of Toasted Almond & Cherry Biscotti after the FDA flagged undeclared Red 40. The recall is classified as high hazard. Consumers should avoid the product and contact the company for refunds or replacements.

Gina Marie Bakery
Undeclared Red
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Food & Beverages
HIGH
FDA FOOD

Gina Marie Bakery Italian Sesame Cookies Recalled for Undeclared Sesame and Food Colorings (2025)

Gina Marie Bakery LLC recalled 172 cases of Italian Sesame Cookies after discovering undeclared sesame and artificial colorings. The recall began with CT state actions and was notified to FDA on 09/10/2025 with customer notification on 09/11/2025. Consumers should not eat these cookies and should seek refunds or replacements.

Gina Marie Bakery
Undeclared Sesame,
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Food & Beverages
HIGH
FDA FOOD

Gina Marie Bakery Cookies Recalled for Undeclared Red 40 and Yellow 6

Gina Marie Bakery LLC recalls Vanilla with Apricot Jam Cookies due to undeclared artificial colorings Red 40 and Yellow 6. The recall, initiated by the state of Connecticut and notified to the FDA, involves 172 cases at 20 containers per case. FDA-listed recall status is ACTIVE with no reported incidents yet.

Gina Marie Bakery
Undeclared Red
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Health & Personal Care
HIGH
FDA DEVICE

Draeger Atlan A350XL Anesthesia Workstation Recalled for Ventilator Failure Risk (223 Units) in 25+N

Draeger recalls 223 Atlan A350XL anesthesia workstations distributed in 25 states and many countries after reports of piston ventilator failure and mechanical ventilation failures. The recall affects units imported from Draegerwerk AG and Co. KGaA. Stop using the device immediately. Contact Draeger for instructions and patient safety guidance.

Draeger
The device
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Health & Personal Care
HIGH
FDA DEVICE

BioPro Recalls 147 Metal and Ceramic Femoral Heads Over Sterility Packaging Issue

BioPro recalled 147 femoral head components distributed in the US. The devices cover metal cobalt chromium and ceramic heads in sizes 22, 28, 32, 36 and 40 millimeters. The recall cites a packaging defect that could compromise the sterile barrier. If implanted, the loss of sterility could pose infection risk. Hospitals and surgeons should follow BioPro recall instructions immediately.

BioPro
Potential packaging
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Health & Personal Care
HIGH
FDA DEVICE

BioPro Femoral Head Hip Implant Recall 147 Units in 2025 Texas and Michigan

BioPro recalled 147 BioPro Femoral Head hip implant components sold in Texas and Michigan after a packaging defect could compromise sterility. The defect may result in loss of sterility, creating a risk of infection if implanted. Hospitals and clinicians should stop using the devices and await manufacturer instructions.

BioPro
Potential packaging
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Health & Personal Care
HIGH
FDA DEVICE

BioPro Endo Head Ceramic Recall Affects 147 Units Over Sterility Packaging Issue (2025)

BioPro recalled 147 Endo Head Ceramic implant components distributed in Texas and Michigan after packaging could compromise the sterile barrier. The defect could result in loss of sterility of the device, creating an infection risk if implanted. Clinicians and patients should stop using the devices and contact BioPro for instructions and refunds.

BioPro
Potential packaging
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Health & Personal Care
HIGH
FDA DEVICE

Iantrek C-Rex UNO CRX-120 Goniotomy Instrument Recalled for Packaging Integrity Issue (2025)

Iantrek recalled 198 C-Rex UNO Microinterventional Goniotomy Instruments, CRX-120 models, distributed nationwide to healthcare facilities. The recall cites potential compromised integrity of the sterile packaging. Healthcare providers and patients should stop using the device immediately and follow recall instructions via the manufacturer.

Iantrek
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Philips Ultrasound OMNI II TEE Transducer Recall Two Units Nationwide (2025)

Philips Ultrasound recalled 2 units of the Philips OMNI II TEE Ultrasound Transducer sold nationwide through multiple retailers. The recall seeks labeling clarification to define the transducer's useful life. Healthcare facilities should stop using the devices and follow Philips recall instructions.

Philips Ultrasound
To provide
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Health & Personal Care
HIGH
FDA DEVICE

GE Medical Systems AW Server 2.0, AW Server 3.0, 3.1, 3.2 Recalled For Security Breach Risk (2025)

GE Medical Systems recalled 7,302 AW Server models worldwide, including 1,381 units in the U.S., after identifying a security vulnerability that could expose patient data. The defect could allow a malicious actor to compromise confidentiality, integrity and availability of information. Healthcare providers should stop using the devices immediately and follow manufacturer instructions for recall.

GE Medical Systems
Firm has
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Tag Statistics

Total Recalls
915

Related Tags

chemical hazardimmediate actionreturn for refundsuffocation riskinfant producttoddler productelderly productplasticmetalelectrical hazardfederal law violationcpsc regulated