MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE Micro-Kill Bleach Germicidal Bleach Wipes
Micro-Kill Bleach Wipes contain out of specification (low) levels of Sodium Hypochlorite.
Read the official notice →- Date
- 2022-03-09
- Country
- United States
- Brand
- MEDLINE INDUSTRIES, LP - Northfield
- Product
- MEDLINE Micro-Kill Bleach Germicidal Bleach Wipes
- Classification
- Class II
- Units
- Worldwide distribution - US Nationwide and the countries of Panama and Bermuda.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 MEDLINE INDUSTRIES, LP - Northfield recalls
- 2022-04-20
US
MEDLINE INDUSTRIES, LP - Northfield recalls Stanbio TDM/Beta-Hydroxybutyrate Linearity Standards, packaged in boxes containing Levels 1-6, 1 x 4 mL each, REF 2450-604,…
The product was stored incorrectly due to improper storage controls which may lead to delayed results.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldDistribution was made to AL, FL, NE OH, TX, WA, and WI. There was no…Official notice →US
MEDLINE INDUSTRIES, LP - Northfield recalls Hydroxybutyrate LiquiColor Tests - includes 3 bottles (1 of each size, 3mL, 8.5mL, and 50mL)
Product was improperly store which may cause a delay in results.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS distribution only - AL, CA, FL, GA, IL, IN, LA, MO, MS, NC, NE, NY, OH, PA,…Official notice →- 2022-04-13
US
MEDLINE INDUSTRIES, LP - Northfield recalls Excelsior Medical 10mL Sterile Field Saline Flush ZR, 0.9% Sodium Chloride Injection, USP, REF EMZ10091280, Sterile, IV…
Sterility failure of the exterior of the syringe which may impact the device's ability to be laid on a sterile field.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide Distribution was made to KY, OK, and TX. There was no…Official notice →- 2022-03-02
US
MEDLINE INDUSTRIES, LP - Northfield recalls meridian bioscience immunocard STAT! Rotavirus test, REF 750030, 30 tests/kit box. The ImmunoCard STAT! Rotavirus…
The product was incorrectly shipped at room temperature rather than refrigerated.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Distribution was made to IL, FL, LA, MS, NC, OH, and TX.Official notice →US
MEDLINE INDUSTRIES, LP - Northfield recalls Michels Transport Medium, 20ML Prefilled Cont
Product stored incorrectly in temperature controlled setting instead of refrigeration.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the states of Colorado, Florida, New York, North…Official notice →- 2022-02-16
US
MEDLINE INDUSTRIES, LP - Northfield recalls CURAD REUSABLE GEL HOT/COLD PACK
The product contains natural rubber latex but the label states that it does not.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS and Bahamas, Bermuda, Panama, Lebanon, Barbados, Honduras, AnguillaOfficial notice →
Other drugs & medical recalls in the United States
- 2022-03-09
US
Microbiologics Inc recalls QC Sets and Panels: KWIK-STIK Cepheid Smart GBS QC Set (Live Culture). Sets include: 1. 0864E4 Streptococcus agalactiae (Group B, lb)…
The Lactobacillus acidophilus negative control (item 0243 single KWIK-STIK) contained in the 8164 Cepheid Xpert GBS QC Set and 8165 Cepheid Smart GBS QC Set was found to test positive for Group B Streptococcus (GBS) in…
FDA · DeviceMicrobiologics IncUS Nationwide distribution in the states of AZ, CA, CO, FL, GA, HI, IA, IL,…Official notice →US
Intuitive Surgical, Inc. recalls da Vinci Xi and X 12-8 mm Conductive Cannula Reducer, REF: 470381-11
Conductive Cannula Reducer metal tip may get dislodged from the plastic shaft. If unnoticed, additional surgery may be required to remove the metal tip. If the procedure proceeds without the metal tip, there is…
FDA · DeviceIntuitive Surgical, Inc.Worldwide distribution - US Nationwide distribution in the states of…Official notice →US
Microbiologics Inc recalls Microbiologics QC Sets and Panels: Helix Elite. Extended Enteric Bacterial Verification Panel (Inactivated Pellet) includes 21 pellets…
Real-time shelf life testing failed at 24 months
FDA · DeviceMicrobiologics IncWorldwide distribution - US Nationwide distribution in the states of AK, CA,…Official notice →US
ROi CPS LLC recalls Regard, TOTAL HIP - SPRINGFIELD, Item No. 8800297010, Case Quantity: 2, Sterile
Products are mislabeled with the incorrect product identification on individual kit labeling.
US
Beckman Coulter Inc. recalls AU/DxC AU Magnesium, Catalog/REF Number OSR6189, UDI 15099590010850
Lipemic interference for the Magnesium serum application failed to meet the performance claim as defined in the IFU. Use may cause a maximum positive bias up to 30.38% in low magnesium patient samples. The impact is…
FDA · DeviceBeckman Coulter Inc.US: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut,…Official notice →US
BioPro, Inc. recalls Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC M/L, Part ID 17037
There is an incorrect statement regarding MR Compatibility in the BioPro Titanium MPJ implant IFU (IFU BP102303 rev 05) and patient implant cards (22266 rev 00) which indicates that the BioPro MPJ Implant has been…
FDA · DeviceBioPro, Inc.US Nationwide distribution in the states of CT, KY, NM, PA, TN, and SD.Official notice →