immediate action Recalls

2,715 recalls tagged with “immediate action”.

Recalled Cordless Grease Gun and location of Serial No.
MEDIUM
CPSC

Makita Recalls Cordless Grease Guns Over Laceration Hazard

Makita U.S.A., Inc. recalled cordless grease guns and hoses on September 4, 2025. The recall affects models XPG01S1, XPG01SR1, and XPG01Z due to a laceration hazard. Consumers should stop using the products immediately and contact Makita for a free replacement.

Makita
The flexible
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Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems Recalls Medical Kits Over Sterilization Risk

American Contract Systems recalled 32,433 medical convenience kits after multiple sterilization cycles compromised product safety. The recall, announced on September 4, 2025, stems from nonconformance during Ethylene Oxide gas sterilization. Affected products include kits used for cataract and eye procedures.

American Contract Systems
Identified products
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Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems Biopsy Tray Recalled Over Sterilization Issues

American Contract Systems recalled 32,433 Basic Biopsy Trays on September 4, 2025. The recall resulted from products being re-gassed after a sterilization failure. The company cannot confirm the safety or effectiveness of these devices after multiple sterilization cycles.

American Contract Systems
Identified products
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Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems Recalls Medical Kits Over Sterilization Issues

American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025. The products failed to meet sterilization standards after being re-gassed improperly. Health providers and patients must stop using these devices immediately.

American Contract Systems
Identified products
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Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems Recalls Medical Kits Over Sterilization Issues

American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025. The recall affects various models due to improper sterilization processes. Patients and healthcare providers must stop using these products immediately.

American Contract Systems
Identified products
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Food & Beverages
HIGH
FDA FOOD

Pacific Coast Producers Recalls Canned Pears Due to Lead Contamination

Pacific Coast Producers recalled 2,436 cans of sliced pears on September 4, 2025. The canned pears may contain lead, posing a significant health risk. Consumers should not consume these products and follow the recall instructions immediately.

Pacific Coast Producers
Potential contamination
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Food & Beverages
HIGH
FDA FOOD

Good and Gather Burrito Bowl Blend Recalled for Undeclared Shrimp

Good and Gather recalled 57,240 bags of Southwest-Style Burrito Bowl Blend on September 4, 2025. The product may contain undeclared shrimp, posing a serious risk to those with shellfish allergies. Consumers should not consume the product and contact ONE FROZEN for refunds or replacements.

ONE FROZEN
Product may
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Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems Recalls Biopsy Trays Due to Sterilization Issues

American Contract Systems recalled 32,433 biopsy trays on September 4, 2025. The recall affects multiple models due to improper re-sterilization that raises safety concerns. Healthcare providers and patients must stop using these products immediately.

American Contract Systems
Identified products
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Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems Recalls Radiology Packs Over Sterilization Issues

American Contract Systems recalled 32,433 radiology packs on September 4, 2025, due to improper sterilization. The products were re-gassed after a nonconformance in the initial Ethylene Oxide gas injection process. Their safety and effectiveness remain unverified after multiple sterilization cycles.

American Contract Systems
Identified products
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Health & Personal Care
HIGH
FDA DEVICE

Lutronic Recalls Electrosurgical Unit Due to Defect Risks

Lutronic recalled 7,490 units of the XERF EFFECTOR 60 electrosurgical unit on September 4, 2025. Manufacturing defects may lead to adverse events for patients. Devices manufactured between April 1, 2025, and August 20, 2025, are affected.

Lutronic
Manufacturing defects
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Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems Recalls Medical Kits Over Sterilization Issues

American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025. The recall follows issues with multiple sterilization cycles that compromise product safety. Patients and healthcare providers should stop using these devices immediately.

American Contract Systems
Identified products
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Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems Recalls Medical Kits Over Safety Risk

American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025. These kits failed to meet safety standards due to improper sterilization processes. The recall affects multiple states, including South Dakota and Iowa.

American Contract Systems
Identified products
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Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems Recalls Medical Kits Over Sterilization Issues

American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025. The products failed to meet sterilization standards, posing a safety risk. Healthcare providers and patients must stop using these kits immediately.

American Contract Systems
Identified products
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Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems Recalls Medical Convenience Kits Due to Hazard

American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025, after discovering re-gassing issues. The affected products have not been validated for safety and effectiveness after multiple sterilization cycles.

American Contract Systems
Identified products
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Health & Personal Care
HIGH
FDA DEVICE

American Contract Systems Recalls Medical Kits Over Sterilization Issues

American Contract Systems recalled 32,433 medical convenience kits on September 4, 2025. The recall follows the identification of products that were re-gassed after sterilization failures. The safety and effectiveness of these products cannot be confirmed due to multiple sterilization cycles.

American Contract Systems
Identified products
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Food & Beverages
HIGH
FDA FOOD

Wegmans Recalls Fruit Cocktail Due to Lead Contamination Risk

Wegmans Food Markets recalled 609 cases of Fruit Cocktail on September 4, 2025, due to potential lead contamination. The affected product includes diced peaches and pears, distributed across multiple states. Consumers should not consume the recalled product and seek a refund or replacement.

Pacific Coast Producers
Potential contamination
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