infant product Recalls

794 recalls tagged with “infant product”.

Food & Beverages
HIGH
FDA FOOD

Middlefield Original Cheese Cooperative Smoked Cheddar Recalled for Listeria Risk in 2025

Middlefield Original Cheese Cooperative recalled 364.125 cases of Smoked Cheddar loaves sold through multiple retailers in Ohio, Pennsylvania, Wisconsin and Texas after a Listeria monocytogenes concern. The recall is Class I and carries a high hazard. Consumers who bought this product should not consume it and should contact the cooperative for refund or replacement information.

Middlefield Original Cheese Cooperative
Potential contamination
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Health & Personal Care
HIGH
FDA DRUG

B. Braun Medical 3000 mL Saline Irrigation Bags Recalled for Sterility Concerns

B. Braun Medical Inc. recalled 16,228 3000 mL saline irrigation bags nationwide in the United States. The recall cites lack of assurance of sterility due to port misalignment, creating a potential for fluid leakage. Healthcare providers and patients should stop using the product immediately and contact the company for guidance.

B. Braun Medical Inc.
Lack of
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Food & Beverages
HIGH
FDA FOOD

Country Eggs Shell Egg Recall Affects 81,542 Dozen Across CA and NV

Country Eggs LLC recalled 81,542 dozen shell eggs distributed to 11 consignees in California and Nevada due to potential salmonella contamination. The recall covers Nagatoshi, Nijiya, Mizuho, and Sunshine yolk varieties sold in large AA Brown egg cartons. Consumers should not eat these eggs and should seek refund or replacement.

Country Eggs
Shell egg
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Health & Personal Care
HIGH
FDA DRUG

Kroger 70% Isopropyl Alcohol Recall Expands for Cross-Contamination Risk

Kroger 70% isopropyl alcohol recall active nationwide, 1860 bottles involved. The recall covers Kroger-branded rubbing alcohol distributed by The Kroger Co. No injuries are reported in the notice. Consumers and healthcare providers should stop using the product immediately and seek guidance from a healthcare professional.

Kroger
Cross Contamination
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Health & Personal Care
HIGH
FDA DEVICE

LeMaitre Vascular Artegraft 10-Unit Recall 2025 for Labeling Errors

LeMaitre Vascular recalls 10 Artegraft Collagen Vascular Grafts distributed internationally to Great Britain and Switzerland, with no US distribution. The devices were labeled incorrectly and lacked CE and UKCA marks and missing patient documents. Healthcare providers and patients should stop using the devices and follow recall instructions immediately.

LeMaitre Vascular
Devices were
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Health & Personal Care
HIGH
FDA DRUG

Ultra Violette Velvet Screen SPF 50 Sunscreen Recalled for SPF Inconsistency; 49,275 Tubes Affected

FDA-listed recall covers 49,275 tubes sold nationwide. Ultra Violette Velvet Screen Blurring Mineral Skinscreen distributed by Grace & Fire USA Inc. Tested SPF results ranged from 4 to 64. Consumers should stop using the product immediately and contact Grace & Fire USA for guidance.

ULTRA VIOLETTE VELVET SCREEN BLURRING MINERAL SKINSCREEN
Subpotent/Super-potent Product:
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Health & Personal Care
HIGH
FDA DEVICE

CooperVision Recalls 180 Softmed Breathables Toric Lenses Over Invalid Sterilization Cycle (2025)

CooperVision recalled 180 Softmed Breathables toric daily disposable contact lenses after one lot was manufactured with an invalid sterilization cycle. The lenses were distributed across Florida, Kentucky, North Carolina and Wisconsin. Patients should stop using the affected lenses immediately and follow the recall instructions.

CooperVision
One lot
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Vehicles & Parts
HIGH
NHTSA

Ford 2025-2026 F-Series Recalled for Instrument Panel IPC Start-Up Failure (25S88)

Ford is recalling certain 2025-2026 F-550 SD, F-450 SD, F-350 SD, F-250 SD, and 2025 F-150 vehicles because the instrument panel may fail at startup. The recall covers 2025-2026 models. Ford will provide an IPC software update via dealer service or OTA at no cost. Owner letters were mailed September 5, 2025. Contact Ford customer service at 1-866-436-7332. Recall number 25S88.

Ford
An instrument
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Health & Personal Care
HIGH
FDA DEVICE

CooperVision Voyant 1-Day Premium Toric Contact Lens Recalled for Invalid Sterilization Cycle

CooperVision recalled one lot of Voyant 1-Day Premium Toric contact lenses sold nationwide in the United States after an invalid sterilization cycle was detected. The recall affects 90 units distributed in Florida, Kentucky, North Carolina and Wisconsin. Patients should stop using the lenses immediately and contact their eye care professional for guidance.

CooperVision
One lot
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Health & Personal Care
HIGH
FDA DEVICE

Abbott i-STAT CG4+ Cartridge Recall: 9,067,050 Units Across U.S. With 510(k) Clearance Issue (2025)

Abbott Point Of Care recalled 9,067,050 i-STAT CG4+ cartridges sold nationwide in the United States. The recall cites a lack of 510(k) premarket clearance to reflect updated sample type for lactate and measurement ranges for pH and PO2. Patients and healthcare providers should stop using the device immediately and follow manufacturer instructions.

Abbott Point Of Care
Lack of
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Health & Personal Care
HIGH
FDA DEVICE

Frontier Devices 301.912S1 12 mm Distraction Pin Recall Expanded to 3,790 Units (Rx Only)

Frontier Devices recalled 3,790 units of the 12 mm Distraction Pin, REF 301.912S1, distributed nationwide in the United States. The recall cites labeling that includes shelf life which has not been validated. The high-risk device category reflects potential documentation and shelf-life concerns. Healthcare providers and patients should follow recall instructions and contact the manufacturer for a回

Frontier Devices
Labeling includes
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Food & Beverages
HIGH
FDA FOOD

Taylor Farms Retail Salad Kit Recalled for Undeclared Sesame and Soy Allergens (2025)

Taylor Farms Retail issued a Class I recall for 8,284 salad kits after undeclared sesame and soy allergens were found inside a dressing packet. The recall covers products labeled under Taylor FARMS Honey Balsamic Salad Kit sold across 19 states. Consumers should not eat the product and should seek refunds or replacements from Taylor Farms Retail.

Taylor Farms Retail
Undeclared allergens
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Health & Personal Care
HIGH
FDA DEVICE

Frontier Devices 301.916S1 16 mm Distraction Pin Recall Expanded (2025)

Frontier Devices and Folsom Metal Products issued a high-risk recall for 490 units of the 16 mm Distraction Pin, REF 301.916S1, distributed nationwide in the United States. The labeling includes shelf life that has not been validated. Patients and healthcare providers should stop using the device immediately and follow recall instructions.

Frontier Devices
Labeling includes
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Health & Personal Care
HIGH
FDA DEVICE

Bard Peripheral Vascular Venclose DigiRF Generator Recall Affects 1,725 Units Worldwide

Bard Peripheral Vascular recalled 1,725 Venclose digiRF Generators with software version 3.35. The recall centers on a catheter verification feature that can produce false positives and disable compatible EVSRF catheters. The worldwide distribution includes the United States. Patients and healthcare providers should stop using the device and await further instructions from the manufacturer.

Bard Peripheral Vascular
Software version
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Health & Personal Care
HIGH
FDA DEVICE

Abiomed Impella Controller AIC Recall 2025 Affects 71 Units Across 6 Regions

Abiomed’s automated Impella Controller recall covers 71 units distributed across the US and international markets. The devices may have a Pump Driver Circuit Assembly that does not meet current specifications. This can reduce pump performance or trigger a pump stop with alarms. Clinicians and patients should follow manufacturer instructions and contact Abiomed or healthcare providers for guidance.

Abiomed
Specific Automated
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Tag Statistics

Total Recalls
794

Related Tags

fda regulatedcpsc regulatedreturn for refundstop use immediatelyimmediate actionkitchenchemical hazardlithium batterypet relatedreplacement availableholiday productpoisoning risk