🔍 RecallPedia

All Recalls

95,114 total recalls in our database

🍎
28,983
Food
 💊
17,685
Drugs
 🏥
38,779
Medical Devices
 🏠
9,667
Consumer Products

MyChai Chai Tea Concentrate KALI, 68 fl. oz. Product is packaged in plastic (HDPE) 1/2gallon bottle, cap has a foil liner that is induction sealed during the bottling process. Shelf stable 3 year expiration from date of manufacture Ingredients: Water, Sugar, Organic Black Tea Extract, Organic Spices, Molasses, Vanilla Extract, Natural Flavors, Citric Acid. Made by: MyChai, Inc. 1110 SE Centennial St. Suite 6, Bend, OR 97702. USAGE: Mix 1 part chai to 5 parts milk or soy. Up until fall of 2023, expiration dates were 2 years from the date of production. In the fall of 2023 expiration dates were extended an additional year to 3 years from the production date.

My Chai

🍎 Food Class I - Dangerous

Acidified Chai Tea products are recalled because pH was found above 4.1 and lack production record.

Aug 21, 2024 Dairy & Eggs Nationwide View Details →

MySyrup Sugar Free Raspberry Syrup. Product is packaged in the same square 0.5gallon HDPE plastic bottles and the volume is 68 fl oz. Ingredients: Water, natural flavor, vanilla extract, sodium benzoate and potassium sorbate (to protect flavor), sucralose, acesulfame potassium, citric acid. Made by: MyChai, Inc. 1110 SE Centennial St. # 6, Bend, OR 97702. Up until fall of 2023, expiration dates were 2 years from the date of production. In the fall of 2023 expiration dates were extended an additional year to 3 years from the production date.

My Chai

🍎 Food Class I - Dangerous

Acidified product is recalled due to lack production record.

Aug 21, 2024 Beverages Nationwide View Details →

MyChai Chai Tea Concentrate Double. Product is packaged in the same square 0.5 gallon HDPE plastic bottles and have volumes of 68 fl oz. Ingredients: Water, Sugar, Organic Black Tea, Organic Spices, Molasses, Vanilla Extract, Citric Acid, Natural Flavors. Made by: MyChai, Inc. 1110 SE Centennial St. Suite 6, Bend, OR 97702. USAGE: Add this jug to 0.5 gallon water, then use 1:1 with milk or soy. Up until fall of 2023, expiration dates were 2 years from the date of production. In the fall of 2023 expiration dates were extended an additional year to 3 years from the production date.

My Chai

🍎 Food Class I - Dangerous

Acidified Chai Tea product is recalled due to lack production record.

Aug 21, 2024 Dairy & Eggs Nationwide View Details →

MySyrup Sugar Free Coconut Syrup. Product is packaged in the same square 0.5gallon HDPE plastic bottles and the volume is 68 fl oz. Ingredients: Water, natural flavor, potassium sorbate and sodium benzoate (to protect flavor), sucralose, acesulfame potassium, citric acid. Made by: MyChai, Inc. 1110 SE Centennial St. # 6, Bend, OR 97702. Up until fall of 2023, expiration dates were 2 years from the date of production. In the fall of 2023 expiration dates were extended an additional year to 3 years from the production date.

My Chai

🍎 Food Class I - Dangerous

Acidified product is recalled due to lack production record.

Aug 21, 2024 Beverages Nationwide View Details →

MySyrup Sugar Free Hazelnut Syrup. Product is packaged in the same square 0.5gallon HDPE plastic bottles and the volume is 68 fl oz. Ingredients: Water, natural and artificial flavor, potassium sorbate and sodium benzoate (to protect flavor), sucralose, acesulfame potassium, citric acid. Made by: MyChai, Inc. 1110 SE Centennial St. # 6, Bend, OR 97702. Up until fall of 2023, expiration dates were 2 years from the date of production. In the fall of 2023 expiration dates were extended an additional year to 3 years from the production date.

My Chai

🍎 Food Class I - Dangerous

Acidified product is recalled due to lack production record.

Aug 21, 2024 Beverages Nationwide View Details →

Ibuprofen 800mg, Generic for: Motrin, Each tablet contains: Ibuprofen, USP 800 mg, Packaged and Distributed by: DIRECT Rx, Dawsonville, GA 30534, Mfg By: Dr. Reddy's Laboratories LA, LLC, Shreveport, LA 71106, a) NDC 61919-0621-15 (15 count bottles), b) NDC 61919-0621-30 (30 count bottles, c) NDC 61919-0621-40 (40 count bottles), d) NDC 61919-0621-60 (60 count bottles), e) NDC 61919-0621-90 (90 count bottles), f) NDC: 61919-0621-100 and NDC: 61919-0621-71 (100 count bottles), g) NDC 61919-0621-72 (120 count bottles).

Direct Rx

💊 Drugs Class I - Dangerous

Failed Impurities/Degradation Specifications: Product failed impurity specifications at the 18-month stability testing.

Aug 9, 2024 Prescription Drugs Nationwide View Details →

Hillrom Welch Allyn Vision Express Holter Analysis System; Electrocardiograph

Baxter Healthcare

🏥 Medical Devices Class I - Dangerous

There is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and Communication System (PACS)) relies solely on the UID to accept exams, this could lead to a mismatch of the patients identification with their physiological data.

Oct 11, 2024 Other Medical Devices View Details →

DeRoyal CHILDREN'S LAPTRACEPACK, 89-9362.06

DeRoyal Industries

🏥 Medical Devices Class I - Dangerous

DeRoyal is recalling certain lots of surgical procedure pack products that contain a Stryker SafeAir Smoke Evacuation Pencil. The recall is due to Stryker receiving reports that the pencil is activating without manual input when plugged into a power source or remains active after buttons are released.

Oct 3, 2024 Other Medical Devices Nationwide View Details →

Hillrom Welch Allyn Q-Stress Cardiac Stress Testing System; cardiac stress test

Baxter Healthcare

🏥 Medical Devices Class I - Dangerous

There is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and Communication System (PACS)) relies solely on the UID to accept exams, this could lead to a mismatch of the patients identification with their physiological data.

Oct 11, 2024 Diagnostic Equipment View Details →

Americot 20-01S (1/4" x 1/4") or 6mm x 6mm: Neurological sponges for use in the protection of neural tissue during surgery. Ref: 20-01S ¿ x ¿ inches or 6mm x 6mm) Component: N/A

American Surgical Company

🏥 Medical Devices Class I - Dangerous

Product defect where the X-ray detectable barium strip (aka radio-opaque marker) becomes detached from the sponge (pattie). May delay surgical process as the surgeon may require extra time to remove the markers from the surgical field.

Sep 18, 2024 Other Medical Devices View Details →