DeRoyal Industries Inc recalls DeRoyal Sterile Custom Kits containing ICU Medical MicroClave Clear Connectors
Procedure packs contained a recalled product.
Read the official notice →- Date
- 2022-09-07
- Country
- United States
- Brand
- DeRoyal Industries
- Product
- DeRoyal Sterile Custom Kits containing ICU Medical MicroClave Clear Connectors
- Classification
- Class II
- Units
- US Nationwide distribution in the states of OH and TN.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 DeRoyal Industries recalls
- 2023-01-18
US
DeRoyal Industries Inc recalls DeRoyal ORGAN RECOVERY PACK PGYBK, a) REF 89-9004.09 and b) 89-9004.10
DeRoyal is recalling certain lots of surgical procedure pack products that contain a Medtronic Non-Absorbable Suture. The recall is due to Medtronic determining a manufacturing error in the packaging of the…
FDA · DeviceDeRoyal Industries IncUS Nationwide distribution in the states of IL, MO.Official notice →- 2023-01-11
US
DeRoyal Industries Inc recalls DeRoyal Tonsillectomy Tray, REF 89-10698.01
DeRoyal is recalling certain lots of surgical procedure pack products that contain a ConMed Foot Controlled Electrosurgical Suction Coagulator. The recall is due to ConMed receiving reports that the suction ports may…
- 2022-12-21
US
DeRoyal Industries Inc recalls DeRoyal MYELOGRAM PACK, REF 89-9304.05
XXX
FDA · DeviceDeRoyal Industries IncUS: Tennessee, Texas, New York, Wisconsin, Florida, Virginia, Massachusetts,…Official notice →US
DeRoyal Industries Inc recalls DeRoyal CATARACT PACK CSM, REF 89-6863
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
FDA · DeviceDeRoyal Industries IncUS: Tennessee, Texas, New York, Wisconsin, Florida, Virginia, Massachusetts,…Official notice →- 2022-08-31
US
DeRoyal Industries Inc recalls DeRoyal limb holders: (1) DeRoyal Limb Holder, Wrist, Fixed, Quick Release, REF M8124; (2) DeRoyal Limb Holder, Ankle, Fixed, Quick…
The webbing strap was laced improperly through the teeth of the buckle allowing the webbing strap to slide and was, therefore, not secure.
FDA · DeviceDeRoyal Industries IncUS Nationwide distribution in the states of FL, IN, NV, RI, TN, TX, and WV.Official notice →- 2022-04-13
US
DeRoyal Industries Inc recalls DeRoyal Ultra/Mammo Tray, containing Prevantics antiseptic (chlorhexidine gluconate and isopropyl alcohol) swab, for preparation of the…
A kit component, the PDI Prevantics Swab was recalled due to uncertain validation of test methods used to manufacture the products.
FDA · DeviceDeRoyal Industries IncUS distribution to Florida, New Jersey, and TennesseeOfficial notice →
Other drugs & medical recalls in the United States
- 2022-09-14
US
Plastikon Healthcare LLC recalls MILK OF MAGNESIA USP, 2400 mg/30 mL, Magnesium Hydroxide, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For…
Microbial Contamination of Non-Sterile Products
- 2022-09-07
US
Oculus Optikgeraete GMBH recalls Pentacam AXL REF 70100, Pentacam HR REF 70900. Used to image the anterior segment of the eye.
Due to a software issue, IOL calculator printout often does not accurately reflect the alignment axis and incision position when planning toric IOLs
FDA · DeviceOculus Optikgeraete GMBHU.S.: AL, AR, AZ, CAQ, CO, CT, FL, GA, HI, IA, ID, IL, KS, KY, MD, ME, MI, MN,…Official notice →US
Boston Scientific Corporation recalls The PRM is intended to be used as part of the ZOOM LATITUDE Programming System to communicate with Boston Scientific implantable…
There is potential for unanticipated software anomalies to occur when using the Model 2868 Application loaded on the 3120 ZOOM LATITUTDE programmer when communicating with certain Boston Scientific transvenous…
US
Corin Ltd recalls TaperFit Stem, Size 0, 38mm OFFSET, 12/14 Taper + 188.550 Centraliser, For Cemented Use, REF 588.3800. Orthopedic hip implant component.
Some of the devices did not pass fatigue testing.
FDA · DeviceCorin LtdDistribution was made to NJ. There was no military/government distribution.Official notice →US
Canon Medical System, USA, INC. recalls INFX-8000V. For radiographic and fluoroscopic studies and intervention.
The fluoroscopic dose rate might exceed the conforming value during biplane fluoroscopy.
US
Abbott Laboratories recalls ARCHITECT STAT Troponin-I Reagent Kit, REF 2K41-27
One lot of reagent was manufactured with insufficient quantities of the heterophilic blocking agents in the conjugate component.