Teligent Pharma, Inc.’s Issues Voluntary Recall of Lidocaine HCl Topical Solution 4% (Lot # 14218, Exp. 09/2022) Due to Super Potency

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Teligent Pharma, Inc. is voluntarily recalling one lot of Lidocaine HCl Topical Solution 4%, 50ml in a screw cap glass bottle to the user level. The product is being recalled because the firms testing has found it to be super potent based on an Out of Specification (OOS) result obtained at the 18-m

Source: Food and Drugs Administration--Recalls/Safety Alerts

Rocky Top Farms Issues Allergy Alert on Undeclared Milk in “Cherry Butter”

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Rocky Top Farms of Ellsworth, MI, is recalling its 10-ounce jars of "Cherry Butter" fruit butter because they may contain undeclared milk. People who have an allergy or a severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

Source: Food and Drugs Administration--Recalls/Safety Alerts

Rocky Top Farms Issues Allergy Alert on Undeclared Milk in “Cherry Butter”

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Rocky Top Farms of Ellsworth, MI, is recalling its 10-ounce jars of "Cherry Butter" fruit butter because they may contain undeclared milk. People who have an allergy or a severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

Source: Food and Drugs Administration--Recalls/Safety Alerts

Top Quality Dog Food Recalls Batch Of “Beef HVM” 1-Pound Packages with Lot Number 071521, Because of Possible Salmonella, Listeria Monocytogenes Health Risk

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Top Quality Dog Food of Hyattsville, MD is recalling “Beef HVM” 1-pound packages due to the potential of Salmonella spp., Listeria monocytogenes. Salmonella, Listeria, can affect animals eating the product and there is risk to humans handling contaminated products, especially if they have not thor

Source: Food and Drugs Administration--Recalls/Safety Alerts

KBF Inc. Issues Allergy Alert on Undeclared Milk Allergens in Banoful Top Orange Biscuit

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KBF Inc. of Astoria, NY, is recalling its 8.11 ounce packages of “Banoful Top Orange Biscuit” food treats because they may contain undeclared milk allergens. Consumers who are allergic to milk allergens may run the risk of serious or life-threatening allergic reactions if they consume this product

Source: FDA Food Safety Recalls RSS Feed

Baxter Issues Urgent Medical Device Correction for All Spectrum IQ Infusion Pumps to Reinforce Important Safety Information Regarding Best Practices for Customer-Initiated IT Network Updates

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Baxter International Inc. announced today it has issued an Urgent Medical Device Correction for all Spectrum IQ infusion pumps to reinforce important safety information when customers implement changes to their network configuration and server systems. Baxter previously communicated this informatio

Source: Food and Drugs Administration--Recalls/Safety Alerts

Jimbo’s Kitchen, DBA New England Cupboard Issues Allergy Alert on Jimbo’s Bloody Mary Mix

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Jimbo’s Kitchen, DBA New England Cupboard is recalling Jimbo’s Bloody Mary Mix because it contains undeclared soy, wheat and sulfites. People who have an allergy or severe sensitivity to soy, wheat and sulfites run the risk of serious or life-threatening allergic reaction if they consume these produ

Source: FDA Food Safety Recalls RSS Feed

Loki Fish Company Recalls Keta Salmon Lox Because of Possible Health Risk

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Loki Fish Company of Seattle, Washington is recalling 4 oz. packages of Keta Salmon Lox (UPC code 92103 00111) because it has the potential to be contaminated with Listeria monocytogenes

Source: Food and Drugs Administration--Recalls/Safety Alerts

Cardinal Health Issues Nationwide Recall of Select Monoject™ Flush Prefilled Saline Syringes

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On August 4, 2021, Cardinal Health (NYSE: CAH) initiated a nationwide recall of approximately 267 million MonojectTM Flush Prefilled Saline Syringes (0.9% Sodium Chloride). The products have been found to reintroduce air into the syringe after the air has been expelled. This could result in injectio

Source: Food and Drugs Administration--Recalls/Safety Alerts

Pfizer Expands Voluntary Nationwide Recall to include Four Additional Lots of CHANTIX® (varenicline) Tablets Due to N- Nitroso Varenicline Content

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Pfizer is voluntarily recalling an additional four lots of Chantix 0.5mg/1 mg Tablets to the patient (consumer/user) level due to the presence of a nitrosamine, N-nitroso-varenicline, above the Pfizer established Acceptable Daily Intake (ADI) level.

Source: Food and Drugs Administration--Recalls/Safety Alerts