Colgate-Palmolive Recalls Fabuloso Multi-Purpose Cleaners Due to Risk of Exposure to Bacteria
The recalled products can contain Pseudomonas species bacteria, including Pseudomonas aeruginosa and Pseudomonas fluorescens, which are environmental organisms found widely in soil and water. People with weakened…
Read the official notice →
- Date
- 2023-02-08
- Country
- United States
- Brand
- Colgate-Palmolive Company, of New York
- Product
- Fabuloso Multi-Purpose Cleaners
- Units
- About 4.9 million (In addition, about 56,000 in Canada)
- Category
- Drugs & medical
- Source
- CPSC
Copied automatically from the US Consumer Product Safety Commission. Details may be shortened or out of date; the official notice is the authoritative source.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 Consumer Product Safety Commission has the exact models, batch codes and remedy, and it takes priority.
Other drugs & medical recalls in the United States
- 2023-02-08
US
US
US
GFA Production Xiamen Co. Ltd. recalls Adventure Marine 150, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 1015-0150
Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.
- 2023-02-01
US
Biokit, S.A. recalls biokitHSV-2 Rapid Test, REF: 300028001
HSV-2 rapid test may report false positive results.
FDA · DeviceBiokit, S.A.US Nationwide distribution in the states of NY, CA, IN, NC, VA.Official notice →US
SunMed Holdings, LLC recalls Air-Q3 AirQ3 Standard ILA with Manual Cuff Inflation and GA Size REF Number 0.0 50005 0.5 50055 1.0 50105 1.5 50155 2.0 50205 3.0 50305…
There is an orogastric (OG) tube size discrepancy between the labeling in the IFU and the printed text on the device. If the clinician is unable to pass a gastric catheter through one of the channels, the clinician may…
FDA · DeviceSunMed Holdings, LLCUS Nationwide distribution in the states of AL, CA, FL, MI, OH, TN, TX, WA.Official notice →US
Biomet, Inc. recalls Oxford Partial Knee System, Fixed Lateral Tibial Construct- Intended to replace part of a knee joint when used in conjunction with a…
Packaged in the incorrect shelf carton. Incorrect shelf carton; outer carton is smaller than the required outer carton, which forces the Tyvex pouch to be folded and packaged in the carton causing compound creases and…
FDA · DeviceBiomet, Inc.Worldwide distribution - US Nationwide distribution in the states of IN, KY…Official notice →