Dollar Tree Distribution, Inc. recalls Medical Device products purchased from Family Dollar retail stores located in Alabama, Arkansas, Louisiana, Mississippi, Missouri…
Potential exposure to rodents and rodent activity in the distribution center.
Read the official notice →- Date
- 2022-03-30
- Country
- United States
- Brand
- Dollar Tree Distribution
- Product
- Medical Device products purchased from Family Dollar retail stores located in Alabama, Arkansas, Louisiana, Mississippi, Missouri and…
- Classification
- Class II
- Units
- US Nationwide distribution: Alabama, Arkansas, Louisiana, Mississippi,…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Dollar Tree Distribution recalls
- 2023-10-25
USDollar Tree Distribution, Inc. recalls Certain Over-The-Counter (OTC) drug products sold by Family Dollar retail stores.
CGMP Deviations: OTC products were stored outside of labeled temperature requirements.
- 2022-03-09
- US
Dollar Tree Distribution, Inc. recalls Dietary supplements purchased from Family Dollar retail stores located in Alabama, Arkansas, Louisiana, Mississippi, Missouri and…
Potential exposure to rodents and rodent activity in the distribution center.
FDA · FoodDollar Tree Distribution, Inc.Alabama, Arkansas, Louisiana, Mississippi, Missouri and TennesseeOfficial notice → - US
Dollar Tree Distribution, Inc. recalls All Over-The-Counter (OTC) drug products sold by Family Dollar retail stores located in Alabama, Arkansas, Louisiana, Mississippi,…
CGMP Deviations: Potential exposure to rodents and rodent activity in the distribution center.
FDA · DrugDollar Tree Distribution, Inc.Alabama, Arkansas, Louisiana, Mississippi, Missouri, TennesseeOfficial notice →
Other drugs & medical recalls in the United States
- 2022-03-30
- US
Dignitana, Inc. recalls DigniCap Delta Scalp Cooling System, Product Number: 900-1001, Labeling: The DigniCap Scalp Cooling System User Manual (PN:…
Instructions for Use (IFUs) updated to include use of a headband is now recommended for all patients and instructions for the application of the headband. Additionally, IFU updated to include warnings for risk of…
FDA · DeviceDignitana, Inc.US Distribution to states of: LA, NC, NJ, FL, WI, CA, NY, KS, GA, SC, CT and KY.Official notice → - US
Cytocell Ltd. recalls Cytocell 8 Square Template Slides (Glass)- microscope slides Reference: PCN008
Labelled with an incorrect expiry date on the outer label with an extended expiry date than the validated shelf life. The correct expiry date for the device is 2022-02 and not 2023-05 as shown on the outer label.
- US
Ace Surgical Supply Co., Inc. recalls NuOss Collagen Block Size 8mm x 9mm x 9mm- used in filling periodontal and maxillofacial defects. Catalog Number: 5099250
NuOss Collagen (dental) was packaged with a Collatene Fibrillar Collagen(for oral wounds) rather than NuOss Collagen Block, may result in suboptimal bone repair
FDA · DeviceAce Surgical Supply Co., Inc.Worldwide distribution - US Nationwide distribution in the states of GA, NY,…Official notice → - US
Baxter Healthcare Corporation recalls Compella Therapy Air Supply Unit
Potential damage to the power cord may cause the power conductors to be exposed, thereby creating a risk of shock from the power mains.
FDA · DeviceBaxter Healthcare CorporationWorldwide distribution - US Nationwide and the countries of Australia,…Official notice → - US
B Braun Medical Inc recalls PERFUSOR SPACE - US VERSION. Intended Use: syringe infusion pump that can be used to configure customized, tailor-made solutions Catalog…
Units not properly inspected prior to release to the market, may not function as indicated in the product labeling, resulting in syringe detection and infusion accuracy that can result in delays in therapy,…
- US
Integra LifeSciences Corp. recalls Codman Cranial Access Kits- indicated when a craniotomy is required for placement of an intracranial pressure (ICP) monitoring device…
Incorrect extended expiration dates identified on the outer box label only, if product is used past the correct expiration date there is a potential for pain, infection, or adverse tissue reaction to occur
FDA · DeviceIntegra LifeSciences Corp.Worldwide distribution - US Nationwide and the country of Hong Kong.Official notice →