chemical hazard Recalls

1,078 recalls tagged with “chemical hazard”.

Health & Personal Care

HIGH

FDA DRUG

Fresenius Kabi 5% Dextrose Injection Recall for Sterility Concerns (2026) Affecting US Nationwide, R

Fresenius Kabi USA, LLC recalls 5% Dextrose Injection, USP IV solution in freeflex bags due to lack of assurance of sterility. The recall affects batches 6402399, 6402400, and 6402401 with Exp 02/28/2027. Distributors nationwide, including Alaska and Puerto Rico, are notified. Stop using and contact the company for guidance and potential replacement.

Mar 11, 2026

DEXTROSE

Lack of

Health & Personal Care

HIGH

FDA DRUG

Fresenius Kabi 0.9% Sodium Chloride Injection Recalled for Lack of Sterility Assurance (2026)

Fresenius Kabi USA recalled 0.9% Sodium Chloride Injection nationwide, including Alaska and Puerto Rico. The recall is due to lack of assurance of sterility. Healthcare providers should stop using the product immediately and contact Fresenius Kabi for guidance.

Mar 11, 2026

SODIUM CHLORIDE

Lack of

Health & Personal Care

HIGH

FDA DRUG

Fresenius Kabi 0.9% Sodium Chloride Injection Recalled for Lack of Sterility Assurance

Fresenius Kabi USA recalls 0.9% Sodium Chloride Injection units distributed nationwide, including Alaska and Puerto Rico. The recall cites lack of assurance of sterility. Healthcare providers should stop use and contact Fresenius Kabi for guidance.

Mar 11, 2026

SODIUM CHLORIDE

Lack of

Health & Personal Care

HIGH

FDA DRUG

BD and Fresenius Kabi 1,000 mL Sodium Chloride Injection Recall for Sterility Concerns (2026)

BD and Fresenius Kabi recall 1,000 mL sodium chloride injection due to lack of assurance of sterility. The U.S. distribution covers nationwide, Alaska, and Puerto Rico. Health care providers should stop use and seek guidance from Fresenius Kabi or a clinician immediately.

Mar 11, 2026

SODIUM CHLORIDE

Lack of

Health & Personal Care

HIGH

FDA DRUG

Fresenius Kabi Saline Solution Recalled for Lack of Sterility Assurance (2026)

Fresenius Kabi USA recalled saline injections distributed nationwide, including Alaska and Puerto Rico. The action covers multiple batch numbers with sterility concerns. Healthcare providers and patients should stop using the product immediately and follow official guidance for replacement options.

Mar 11, 2026

SODIUM CHLORIDE

Lack of

Health & Personal Care

HIGH

FDA DRUG

BD and Fresenius Kabi Sodium Chloride Injection Recalled for Lack of Sterility Assurance (2026)

BD Becton, Dickinson and Company and Fresenius Kabi USA recall 0.9% Sodium Chloride Injection, USP, 250 mL in a single-dose bag nationwide, including Alaska and Puerto Rico. The recall cites lack of assurance of sterility. Healthcare providers and patients should stop using the product immediately and follow guidance from Fresenius Kabi or their provider.

Mar 11, 2026

SODIUM CHLORIDE

Lack of

Health & Personal Care

HIGH

FDA DRUG

Fresenius Kabi 5% Dextrose Injection Recall Active Over Sterility Assurance Issue (2026)

Fresenius Kabi USA, LLC recalled 5% Dextrose Injection, USP, 50 mL in a 100 mL freeflex bag, distributed nationwide including Alaska and Puerto Rico. The recall cites lack of assurance of sterility. Consumers and healthcare providers should stop using this product immediately and contact Fresenius Kabi for guidance.

Mar 11, 2026

DEXTROSE

Lack of

Health & Personal Care

HIGH

FDA DRUG

Fresenius Kabi 5% Dextrose Injection Recalled for Lack of Sterility Assurance (2026)

Fresenius Kabi USA, LLC recalls 5% Dextrose Injection, USP 12.5 g per 250 mL in FreeFlex bags due to lack of sterility assurance. The recall covers units distributed nationwide including Alaska and Puerto Rico. Healthcare providers and patients should stop use and consult a healthcare professional.

Mar 11, 2026

DEXTROSE

Lack of

Health & Personal Care

HIGH

FDA DRUG

Zydus Icosapent Ethyl Capsules Recalled for Oxidized Ingredient in 60,541 Bottles (2026)

Zydus Pharmaceuticals USA Inc. is recalling 60,541 bottles of Icosapent Ethyl Capsules, 1 g, 120 capsules per bottle, distributed nationwide in the United States. The recall cites oxidized Icosapent Ethyl causing red dots inside capsules and melted capsules. Patients should stop using the medicine immediately and contact Zydus Pharmaceuticals USA Inc. or their clinician for guidance.

Mar 9, 2026

ICOSAPENT ETHYL

Failed Tablet/Capsule

Health & Personal Care

HIGH

FDA DEVICE

Cook Medical Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Tray Recalled Over Expired-Lot

Cook Incorporated recalled 441 units of the Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Tray after identifying expiration dates that exceed true shelf life. The recall covers lots with Reference Part Numbers C-PTISY-100-HC-G-NA, C-PTISY-100-UNL-HC-G-NA and C-PTISY-100-UNS-HC-G-NA distributed worldwide. Healthcare providers must stop use and follow manufacturer recall instructions.

Mar 5, 2026

Cook

Products from

Health & Personal Care

HIGH

FDA DEVICE

Cook Medical Arterial Pressure Monitoring Tray Recalled Over Expired Shelf-Life Labeling (Z-1778-202

Cook Medical recalled 20 arterial pressure monitoring trays worldwide after labeling showed expiration dates that exceeded true shelf life. The recall targets two reference part numbers, APMY-2.5-15-0-2.5 and APMY-4.0-21J-1-12. Healthcare providers should stop using affected lots immediately and follow recall instructions.

Mar 5, 2026

Cook

Products from

Health & Personal Care

HIGH

FDA DEVICE

Cook Incorporated recalls Melker Universal Cuffed Emergency Cricothyrotomy Catheter Set for Expired-

Cook Incorporated recalls Melker Universal Cuffed Emergency Cricothyrotomy Catheter Set after lots were labeled with expiration dates that exceed true shelf life. The recall affects two reference parts with multiple UDI and lot numbers. Healthcare facilities should stop use and follow recall instructions.

Mar 5, 2026

Cook

Products from

Health & Personal Care

HIGH

FDA DEVICE

Cook Medical Wayne Pneumothorax Set Recalled for Expired Shelf Life Labels

Cook Incorporated recalls 104 Wayne Pneumothorax Sets worldwide after labeling errors show expiration dates exceeding true shelf life. The recall affects reference parts C-UTPT-1020-WAYNE-IMH and C-UTPT-1400-WAYNE-112497-IMH with order numbers G56532 and G56535. Healthcare providers should stop use immediately and follow recall instructions.

Mar 5, 2026

Cook

Products from

Health & Personal Care

HIGH

FDA DEVICE

Cook Medical Spectrum Central Venous Tray Recalled Over Expired Shelf-Life Labels (2026)

Cook Medical recalled 2,348 Spectrum Central Venous Tray units worldwide due to expiration dates that exceed true shelf life. The recall affects lots labeled with overstated expiration dates. Healthcare providers and patients should stop using the affected devices and follow manufacturer instructions.

Mar 5, 2026

Cook

Products from

Health & Personal Care

HIGH

FDA DEVICE

Cook Medical Spectrum Central Venous Catheter Sets Recalled for Expired Shelf-Life Labels (2026)

Cook Medical recalled 5,080 Spectrum Central Venous Catheter Sets worldwide after labeling that indicated expiration dates beyond the products' true shelf life. The recall alerts patients and healthcare providers to stop using affected lots and follow manufacturer instructions.

Mar 5, 2026

Cook

Products from

Health & Personal Care

HIGH

FDA DEVICE

Cook Medical CTO-6 Micro Wire Guide Recalled Worldwide Over Expired Shelf Life Labels (2026)

Cook Medical recalled 15 CTO-6 Micro Wire Guides sold worldwide after labeling errors extended expiration dates beyond true shelf life. The devices carry Reference Part Number CMW-14-190-6G and Order Number G50786. Healthcare providers were notified to stop use immediately until further instructions.

Mar 5, 2026

Cook

Products from

Health & Personal Care

HIGH

FDA DEVICE

Cook Medical Thal-Quick Chest Tube Tray Recalled for Expiration Dates Exceeding Shelf Life

Cook Medical recalled the Thal-Quick Chest Tube Tray, reference part number C-TQTSY-3200, Order G07242, due to expiration dates that exceed true shelf life. The recall is active and worldwide. The hazard is labeling that misstates shelf life. Patients and healthcare providers should stop using the affected devices immediately and follow Cook’s recall instructions.

Mar 5, 2026

Cook

Products from

Health & Personal Care

HIGH

FDA DEVICE

Tornier Tornier HRS Max Parts Recalled for Mislabeling, Incompatibility (2026)

Tornier recalls 233 surgical parts nationwide in the United States. The items were mislabelled as Tornier HRS Max products. These parts fit the Tornier HRS system only and are incompatible with the Tornier HRS Max system. Clinicians and patients should stop using the affected parts and follow recall instructions.

Mar 5, 2026

Tornier

Affected products

Health & Personal Care

HIGH

FDA DEVICE

Cook Medical Blue Rhino G2-Multi Tracheostomy Introducer Set Recalled for Expiration Date Labeling —

Cook Medical recalled 916 units of the Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Set worldwide after discovering expiration dates exceeded true shelf life. The recall affects multiple reference part numbers and order numbers. Healthcare providers should stop using the device immediately and follow Cook’s instructions for recall notification.

Mar 5, 2026

Cook

Products from

Health & Personal Care

HIGH

FDA DEVICE

Cook Medical Multipurpose Drainage Catheter Recalled Over Expired Labeling in Lots G29775

Cook Incorporated recalled 20 units of its Multipurpose Drainage Catheter reference ULT8.5-38-25-P-CLMS-8-RH-FS distributed worldwide. The recall cites expiration dates that exceed the product’s true shelf life. Healthcare providers and patients should stop using the affected devices immediately.

Mar 5, 2026

Cook

Products from

1 2 3 4 5...54

Tag Statistics

Total Recalls

1,078

chemical hazard Recalls

Tag Statistics

Related Tags