Microbiologics Inc recalls QC Sets and Panels, KWIK-STIK AST-GP (4 Strains) QC Set. KWIK-STIK kit that contains Catalog Number 0959P. In Vitro Diagnostic Control…
Tests returning incorrect susceptible results. High Level Gentamicin Synergy value was out of specification (sensitive) when analyzed on the Vitek 2 AST-GP67 card, and these lots failed the disk diffusion method used…
Read the official notice →- Date
- 2022-02-16
- Country
- United States
- Brand
- Microbiologics
- Product
- QC Sets and Panels, KWIK-STIK AST-GP (4 Strains) QC Set. KWIK-STIK kit that contains Catalog Number 0959P. In Vitro Diagnostic Control…
- Classification
- Class II
- Units
- Worldwide Distribution. US nationwide including Puerto Rico and Guam,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Microbiologics recalls
- 2022-03-09
USMicrobiologics 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 →- 2022-02-23
- US
Microbiologics Inc recalls KWIK-STIK(TM), Quality control kit for culture media, sold as: KWIK-STIK(TM) 2-pack Enterococcus faecalis derived from ATCC(R) 51299(TM)
Some of the KWIK-STIK Catalog #01023P Campylobacter coli, Lot# 1023-05-7, contained an inner label stating the product is Catalog #0919K Haemophilus influenza. The organism has been confirmed to be C. coli, indicating…
FDA · DeviceMicrobiologics IncWorldwide distribution - US Nationwide and the countries of Canada, South…Official notice → - 2022-02-16
- US
Microbiologics Inc recalls LYSO Disk(TM) labeled as containing Actinomyces odontolyticus. Each LYSO Disk" unit contains six lyophilized pellets of a single…
Potential for product labeled as Actinomyces odontolyticus is actually Eggerthella lenta.
FDA · DeviceMicrobiologics IncInternational distribution in the countries of Canada and Germany.Official notice → - US
Microbiologics Inc recalls QC Sets and Panels: KWIK-STIK" 2 Pack. Common Name: QC Sets and Panels GP Comprehensive QC Set. Each KWIK-STIK unit contains a lyophilized…
Potential contamination with Escherichia coli Staphylococcus epidermidis and S. warneri.
FDA · DeviceMicrobiologics IncWorldwide distribution - US Nationwide distribution in the states of AR, AZ,…Official notice → - US
Microbiologics Inc recalls LYFO DISK(TM), LYFO DISK(TM) Streptococcus pneumoniae derived from ATCC(R) 49619(TM). LYFO DISK microorganisms are packaged in a…
Potential contamination with Escherichia coli, Staphylococcus epidermidis and S. warneri.
FDA · DeviceMicrobiologics IncWorldwide distribution - US Nationwide distribution in the states of AR, AZ,…Official notice → - US
Microbiologics Inc recalls KWIK-STIK(TM), Streptococcus pneumoniae derived from ATCC(R) 49619(TM), packaged as follows: a. KWIK-STIK(TM) 2 Pack; b. KWIK-STIK(TM) 6…
Potential contamination with S. epidermidis E. coli and S. warneri.
FDA · DeviceMicrobiologics IncWorldwide distribution - US Nationwide distribution in the states of AR, AZ,…Official notice →
Other drugs & medical recalls in the United States
- 2022-02-16
- US
DePuy Orthopaedics, Inc. recalls ATTUNE REVISION POSTERIOR FEMORAL AUGMENT SZ 9 12MM-intended as a Component in total knee arthroplasty (TKA) revision surgeries Product…
May have adhesive residue on the posterior surface of the femoral augment, if undetected prior to implantation, soft tissue irritation and/or infection may occur.
FDA · DeviceDePuy Orthopaedics, Inc.US Nationwide distribution in the states of TN, TX.Official notice → - US
Becton Dickinson & Co. recalls BD Veritor Plus Analyzer - intended to provide rapid test results in near-patient settings. Catalog Number: 256066
May have the potential to overheat and/or cause fire, the issue can occur when an unauthorized alternative AC power adapter, and not the one provided by BD is used to power the instrument.
FDA · DeviceBecton Dickinson & Co.Worldwide distribution - US Nationwide and the countries of Armenia,…Official notice → - US
GE Healthcare, LLC recalls GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Artist system, nuclear magnetic resonance imaging system.
The magnetic resonance systems could potentially have a cryogen ventilation system that does not meet the venting requirements.
FDA · DeviceGE Healthcare, LLCDistribution was nationwide, including Puerto Rico and the Virgin Islands.…Official notice → - US
Microbiologics Inc recalls QC Sets and Panels: KWIK-STIK" 2 Pack. Common Name: QC Sets and Panels GP Comprehensive QC Set. Each KWIK-STIK unit contains a lyophilized…
Potential contamination with Escherichia coli Staphylococcus epidermidis and S. warneri.
FDA · DeviceMicrobiologics IncWorldwide distribution - US Nationwide distribution in the states of AR, AZ,…Official notice → - US
Microbiologics Inc recalls LYFO DISK(TM), LYFO DISK(TM) Streptococcus pneumoniae derived from ATCC(R) 49619(TM). LYFO DISK microorganisms are packaged in a…
Potential contamination with Escherichia coli, Staphylococcus epidermidis and S. warneri.
FDA · DeviceMicrobiologics IncWorldwide distribution - US Nationwide distribution in the states of AR, AZ,…Official notice → - US
Microbiologics Inc recalls KWIK-STIK(TM), Streptococcus pneumoniae derived from ATCC(R) 49619(TM), packaged as follows: a. KWIK-STIK(TM) 2 Pack; b. KWIK-STIK(TM) 6…
Potential contamination with S. epidermidis E. coli and S. warneri.
FDA · DeviceMicrobiologics IncWorldwide distribution - US Nationwide distribution in the states of AR, AZ,…Official notice →