glass Recalls

160 recalls tagged with “glass”.

Health & Personal Care
HIGH
FDA DEVICE

Ion Beam Applications PROTEUS 235 Recalled for 4 Units Worldwide (2026)

Ion Beam Applications S.A. recalled four PROTEUS 235 proton therapy systems distributed worldwide, including Florida in the United States, and the countries of Italy and Japan. The defect disables the Therapy Safety System's Universal Beam Triggering Interface, so the system may not stop beam delivery if the Healthy Signal from an external gating device is lost. Patients and healthcare providers应该

Ion Beam Applications
It was
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Food & Beverages
HIGH
FDA FOOD

Mangalm Tops GOLD Mango Pickle Recall Over Erucic Acid Adulteration (2026)

Mangalm recalls Tops GOLD Mango Pickle after FDA enforcement flagged potential erucic acid adulteration. The recall covers two UPCs and two can sizes distributed in five Western states. Consumers are urged not to eat the product and to contact Mangalm for refunds or replacements.

Mangalm
Potential adulteration
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Health & Personal Care
HIGH
FDA DEVICE

Instrumentation Laboratory GEM Premier 5000 PAK Recalled for PCSND Warm-Up Errors (30 Units, 2026)

Instrumentation Laboratory is recalling 30 GEM Premier 5000 PAK cartridges distributed worldwide, including the United States. The affected cartridges may experience PCSND errors during warm-up, causing GEM PAKs to eject. Stop using the product and follow recall instructions from the manufacturer for refunds or replacements.

Instrumentation Laboratory
Confirmed customer
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Health & Personal Care
HIGH
FDA DEVICE

Instrumentation Laboratory Recalls 7 GEM Premier 5000 Units Over PCSND Errors (2026)

Instrumentation Laboratory recalled seven GEM Premier 5000 units worldwide, including the US. PCSND errors during warm-up may cause GEM PAK cartridges to eject, potentially delaying results. Healthcare providers using these devices should stop using the affected units and contact IL for instructions and a remedy.

Instrumentation Laboratory
Confirmed customer
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Health & Personal Care
HIGH
FDA DEVICE

Instrumentation Laboratory Recalled 180 GEM Premier 5000 PAK Cartridges for PCSND Errors (2026)

Instrumentation Laboratory recalls 180 GEM Premier 5000 PAK cartridges distributed worldwide after reports of PCSND errors during warm-up. During warm-up, GEM PAKs may eject and require insertion of a new GEM PAK. Hospitals should stop using the affected cartridges and follow the manufacturer's recall instructions.

Instrumentation Laboratory
Confirmed customer
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Health & Personal Care
HIGH
FDA DRUG

Med-Nap Cleansing Towelettes Recall 2026 for CGMP Deviations

Med-Nap Cleansing Towelettes, manufactured by Acme United Corporation, were recalled nationwide on January 20, 2026. The recall cites CGMP deviations in manufacturing for benzalkonium chloride 0.13% towelettes. Consumers and healthcare providers should stop using the product immediately and contact Acme United for guidance.

Med-Nap Cleansing Towelettes
CGMP Deviations
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Health & Personal Care
HIGH
FDA DRUG

Med Nap Cleansing Towelettes Recall Expanded Over CGMP Deviations (2026)

ACME United Corporation recalls Med Nap Cleansing Towelettes, 5"x7" Benzalkonium Chloride 0.13%, distributed nationwide. CGMP Deviations prompted the recall. Stop using the product now and contact ACME United or a healthcare provider for guidance.

MED NAP CLEANSING TOWELETTE
CGMP Deviations
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Food & Beverages
HIGH
FDA FOOD

Frederik's by Meijer Focaccia Bread Recalled for Metal Fragments (2026)

Frederik's by Meijer Slow-Roasted Tomato & Parmesan Focaccia Bread recalled after metal fragments were found in 23,459 cases. The recalls spans Frederik's by Meijer, Fresh & Simple, HT Traders and Trader Joe's focaccia products. The metal fragments were traced to roasted tomatoes from an ingredient supplier. Stop using the product and contact the supplier for refunds or replacements.

Bakkavor
Metal fragments
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Food & Beverages
HIGH
FDA FOOD

Bader Enterprises Recalls Premium Food Jordan Almonds in 2.0 oz & 3.5 oz Packaging (2026 Recall)

Bader Enterprises recalls 60 pounds of Premium Food Jordan Almonds sold in New Jersey and New York. The product contains undeclared wheat and blue color additives. Consumers who purchased the product should not consume it. Contact Bader Enterprises for refund or replacement information via two or more notification methods.

Bader Enterprises
Contains undeclared
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Health & Personal Care
HIGH
FDA DEVICE

Waldemar Link Endo-Model 15-0027/12 Implant Recall 2026 for Detachment Risk

Waldemar Link recalled 1 unit of Endo-Model Replacement Plateau implant component distributed worldwide, including New Jersey. The defect involves a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. Patients and healthcare providers should stop using the device immediately and follow the manufacturer’s recall instructions.

Waldemar Link GmbH & Co. KG
The potential
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Health & Personal Care
HIGH
FDA DRUG

Zydus Pharmaceuticals Recalls Icosapent Ethyl Capsules Over Subpotency

Zydus Pharmaceuticals recalled 22,896 bottles of Icosapent Ethyl capsules on December 30, 2025. The recall stems from leakage and oxidation that may reduce the drug's effectiveness. Consumers should stop using the product immediately and seek guidance from healthcare providers.

Zydus Pharmaceuticals
Subpotent Drug:
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Health & Personal Care
HIGH
FDA DRUG

Aleve 60-Count Pain Relievers Recalled for CGMP Deviations by Gold Star Distribution (2026)

Gold Star Distribution recalls Aleve 60-count pain relievers distributed nationwide due to CGMP deviations and insanitary conditions at its distribution center. Rodent exposure and activity were reported at the facility. Consumers and healthcare providers should stop using the product immediately and contact Gold Star Distribution for guidance.

Aleve
CGMP Deviations:
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Food & Beverages
HIGH
FDA DRUG

Swan White Clear Alcohol Recall by Gold Star Distribution in 2026

Gold Star Distribution recalls Swan White Clear Alcohol, 50% ABV, 16 oz, 12 count, nationwide. FDA enforcement cites CGMP deviations and insanitary distribution-center conditions including rodent exposure. Stop using the product now and contact the distributor or a healthcare provider for guidance.

Swan
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DEVICE

Wondfo Streptococcal A At-Home Self-Test Recalled for FDA Clearance Issues (2026)

Wondfo recalled 188 units of Streptococcal A At-Home Self-Test sold nationwide in the United States after regulators found the device was not FDA-cleared. The recall centers on lack of FDA clearance for safety and effectiveness. Consumers should stop using the test immediately and contact Altruan GmbH or their healthcare provider for instructions.

Wondfo
Product not
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Health & Personal Care
HIGH
FDA DRUG

Imprimis NJOF Recalls Intraocular Injection Over Glass Particles

Imprimis NJOF, LLC recalled 314 boxes of Tri-Moxi+¿ intraocular injections on December 18, 2025. The recall is due to the presence of glass-like particles in the product. Consumers and healthcare providers should stop using the product immediately and contact the company for further guidance.

Imprimis NJOF
Presence of
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