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All product recalls associated with Linvatec Corp..
Total Recalls
1000
Past Year
1000
Class I (Serious)
145
Most Recent
Jan 2026
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
The pouch containing the sterile product is not completely seal on all products. Therefore , the sterility of the device is questionable.
The recall includes electric coil top freestanding ranges and wall ovens. The coil ranges are 30 inches wide with controls in the rear. The wall ovens include the 27- and 30-inch models, with the lower oven controlled by a knob and not self-clean. The upper oven is self-clean. The following models are included in this recall: Freestanding Coil Ranges Hotpoint Brand RB757BH/WH/CH RB536WH/CH RB526H RB525BH/H General Electric Brand JBS27BH/WH/CH/SH JBS03BH/H JBS07H JBP21BH/WH Americana Brand ABS300J Kenmore Brand 22-91112/4 22-62781 Double Wall Ovens Kenmore Brand 22-47722/4/9 General Electric Brand JTP28B/W/S/C JKP28B/W/C
Software defect causes patient identification number to be truncated.
Assay may give elevated patients results.
With the Model 8870 software application card versions AAA 02, BBB 04, BBC 02, and BBD 01, which is used in conjunction with the Model 8840 N'Vision Clinician Programmer, users may have mistakenly entered a periodic bolus interval into the minutes field, rather than the hours field, resulting in drug overdoses. This issue is limited to programming the SynchroMed and SynchroMed EL pumps.
The product is contaminated with Burkholderia cepacia (formally known as Pseudomonas cepacia), based on the Texas Health Department analysis and also firm's analysis.
Potential for patient burn
Changes in the ARCHITECT B12 Reagent lots may adversely affect the shape of the calibration curve, over time. These changes may produce controls out of range low and similar decreases in patient sample values prior to current expiration of the reagents.
The recalled batteries are used with the 15-inch PowerBook G4 (Aluminum) laptop computer. The batteries, which contain cells manufactured during the last week of December 2003 only, have the model number A1045 and serial numbers that begin with HQ404, HQ405, HQ406, HQ407, or HQ408. The model and serial numbers can be found on a label on the bottom of the battery. The battery is approximately 4 inches long, 3 inches wide, and ¾ inches tall. No other PowerBook or iBook batteries are involved in this recall.
The recalled product is a red folding chair with a metal frame and vinyl padded seat back and base. The chair was sold as a part of a five-piece juvenile table furniture set with a green table, blue chair, yellow chair, green chair, and red chair. Only the red chairs with model numbers 11-88-3E1 and 11-88S3E1 and date codes H3, B4, D4 or E4 printed underneath the seat bottom are included in the recall. "Meco" or "Samsonite" brand names are also printed on the seat label.
Pumps were manufactured with an incorrect circuit board that may cause an increase in the feed rate and flush frequency of fluids.
This recall involves "Windsor" style arm chairs. The chairs measure 40 inches high by 21 inches wide. Made of black wood, the chairs have 9 metal spindles across the rounded back.
The "GET-GO" and "LITTLE GET-GO" children's athletic shoes come in various color combinations and were sold in toddler and pre-school sizes 2C through 3Y. The Nike Swoosh symbol is on the outside and sole of the shoe. All shoes close with a strap. The style name "GET-GO" or "LITTLE GET-GO" is written on the shoe box. The recalled shoes have one of the following six-digit numbers on a label inside the shoe just above the UPC code: 308638, 308639, 308642 and 308647. Only these style numbers are included in this recall.
The scented candle is housed in a clear glass holder and has a crumbled appearance with color variations. It contains slices of dried apple and cinnamon sticks in the wax. The candle is 3 inches in diameter and 3.5 inches high. "Kitchen Krumblers" is labeled at the base of the candle. The candle was sold separately or in a set with another candle not involved in this recall.
Locking pins may be installed backward, and cot may drop from highest to lowest position when the users are not prepared for the drop.
Devices for which sterility may be compromised as evidenced by a loss of package integrity.
Potential that product is incorrectly assembled with monel wire attached to the tip dome rather than copper wire.
Design change to uppgrade reliability of powered adjustable bed.
These down-rod-mount, dual-motor, 36-inch ceiling fans were sold in chrome, stone white, brush nickel, polished brass, antique brass, or weathered patina finishes. Model number 355-6645 is printed on the box and on a label located on the central housing of the ceiling fan. The brand names of the fans are "Aire Tek" and "Turn-of-the- Century Apollo Series" which is written on the packaging only. A label located on the central housing of the ceiling fan displays the File Number "E215078," the UL Listing Mark, and the model number 355-6645. Vaxcel had previously recalled the same model fan sold under the "Aire Tek" brand name.
Beckman Coulter has confirmed an issue associated with the predilute mode of the COULTER LH 500 Hematology Analyzer. The workstation may display, transmit, and / or print an erroneous result or an incorrect dilution factor with a predilute sample result.