State

Utah product recalls

73,833 recalls have nationwide distribution and so reach Utah. 4,916 additional recalls listed Utah specifically in their distribution scope.

What the numbers show

Total: 4,916
Critical: 524
Severe: 1,351
Most recent: 2026-11-04

Of the 4,916 recalls naming Utah we have scored against our rubric, 524 (11%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,351 (27%) are Severe.

Which agencies issued them

These figures cover only the 4,916 recalls whose distribution notice names Utah specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53426–53450 of 78749

ModerateFDA (Devices)·Z-1104-2016·2016-03-23
Zimmer Manufacturing Recalls Sterile Bone Fixation Screws Due to Calibration Issues
Zimmer Manufacturing B.V. is recalling 12 sterile bone fixation screws due to insufficient sealer calibration data. The products were distributed nationwide in the US.
Product
Product 6 consists of all products under product code HWC, and same usage: Item no: 47493501001 3.5 X 10 CORT SCREW SELFT 47493501801 3.5 X 18 CORT SCREW SELFT Product Usage: A smooth or threaded metallic bone fixation fastener is a device intended to be implanted that…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1138-2016·2016-03-23
Zimmer Manufacturing Recalls Anti-Rotation Screws Due to Sealer Calibration Issues
Zimmer Manufacturing B.V. is recalling seven ITST Anti-Rotation Screws because of insufficient sealer calibration data. The affected sterile products were distributed nationwide in the US.
Product
Product 40 consists of all product under product code: HSB and same usage: Item no: 225706565 ITST ANTI-ROTATION SCREW 225707065 ITST ANTI-ROTATION SCREW 225708065 ITST ANTI-ROTATION SCREW 225708565 ITST ANTI-ROTATION SCREW 225709065 ITST ANTI-ROTATION SCREW Product…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1127-2016·2016-03-23
Zimmer Manufacturing Recalls Sterile Femoral Heads Due to Sealer Calibration Issues
Zimmer Manufacturing B.V. is recalling specific sterile femoral heads used in hip arthroplasty due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.
Product
Product 29 consists of all product under product code: LPHand same usage: Item no: 32902603800 FEMORAL HEAD +0.5 X 22 MM 32902604810 FEMORAL HEAD +3.5 X 22 MM 32902604845 FEMORAL HEAD +7.0 X 22 MM For use in total or hemi hip arthroplasty
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1105-2016·2016-03-23
Zimmer Manufacturing Recalls Sterile Cortical Screws Due to Sealer Calibration Issues
Zimmer Manufacturing B.V. is recalling 109 sterile 3.5mm cortical screws due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.
Product
Product 7 consists of all products under product code HWC, and same usage: Item no: 47234801435 3.5MM CORT SCR X 14MM 47234801635 3.5MM CORT SCR X 16MM 47234806535 3.5MM CORT SCR X 65MM 47234807035 3.5MM CORT SCR X 70MM 47234807535 3.5MM CORT SCR X 75MM 47234808035…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1103-2016·2016-03-23
Zimmer Manufacturing Recalls 2.7mm Cortical Screws Due to Sealer Calibration Issues
Zimmer Manufacturing B.V. is recalling 60 sterile 2.7mm cortical screws due to insufficient sealer calibration data. The products were distributed nationwide in the US.
Product
Product 5 consists of all products under product code HWC, and same usage: Item no: 47482701001 2.7MM CORT. SCREW 10MM, S 47482701201 2.7MM CORT. SCREW 12MM, S 47482701401 2.7MM CORT. SCREW 14MM, S 47482701601 2.7MM CORT. SCREW 16MM, S 47482701801 2.7MM CORT. SCREW…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1155-2016·2016-03-23
Zimmer Manufacturing Recalls Pressfit Femoral Stems Due to Sealer Calibration
Zimmer Manufacturing B.V. is recalling sterile pressfit femoral stems used in hip arthroplasty due to insufficient sealer calibration data.
Product
Product 57 consists of all product code: JDI and same usage: Item no: 763401000 PRESSFIT FEM ST FX 10 X 115 763401100 PRESSFIT FEM ST FX 11 X 1 763401200 PRESSFIT FEM ST FX 12 X 1 763401300 PRESSFIT FEM ST FX 13 X 1 763401400 PRESSFIT FEM ST FX 14 X 1 763401500 PRESSFIT…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1151-2016·2016-03-23
Zimmer NexGen Knee Implant Recall Due to Sealer Calibration Issues
Zimmer Manufacturing B.V. is recalling NexGen knee implant components due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.
Product
Product 53 consists of all product under: product code: JWH and same usage: Item no: 597002501 NEXGEN PRECOAT PEG TIB PL 597002502 NEXGEN PRECOAT PEG TIB PL 597003501 NEXGEN PRECOAT PEG TIB PL 597003502 NEXGEN PRECOAT PEG TIB PL 597004501 NEXGEN PRECOAT PEG TIB PL…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1160-2016·2016-03-23
Zimmer Manufacturing Recalls Trilogy Acet Shell Hip Implant Components
Zimmer Manufacturing B.V. is recalling 400 units of Trilogy Acet Shell hip implant components due to insufficient sealer calibration data.
Product
Product 62 consists of all product under product code: LPH and same usage: Item no: 620003620 TRILOGY ACET SHELL 36MM OD MULTI For use in total hip arthroplasty
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1166-2016·2016-03-23
Zimmer Versys Hip Implant Recall Due to Insufficient Sealer Calibration Data
Zimmer Manufacturing B.V. is recalling 1,220 units of Versus hip implants due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.
Product
Product 68 consists of all product under product code: JDI and same usage: Item no: 787101360 VERSYS CEM/REV/CALCAR 13X 787101361 VERSYS CEM/REV/CALCAR 13X 787101362 VERSYS CEM/REV/CALCAR 13X 787101363 VERSYS CEM/REV/CALCAR 13X 787101560 VERSYS CEM/REV/CALCAR 15X…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1167-2016·2016-03-23
Zimmer Versys Cemented Femoral Stem Recall for Calibration Issues
Zimmer Manufacturing B.V. is recalling 13 Versys Cemented Femoral Stems due to insufficient sealer calibration data. The affected sterile products were distributed nationwide in the US.
Product
Product 69 consists of all product under product code: JDI and same usage: Item no: 785301701 VERSYS CEMENTED FEM STEM 785301521 VERSYS CEMENTED FEM STEM 15X140MM X-OFF 785301601 VERSYS CEMENTED FEM STEM 16X145MM For use in total or hemi hip arthroplasty
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1118-2016·2016-03-23
Zimmer Manufacturing Recalls Compression Screws Due to Sealer Calibration Issues
Zimmer Manufacturing B.V. is recalling 3,415 sterile compression screws due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.
Product
Product 20 consists of all prod oct under poduct code: KTT and same usage: Item no: 47116201900 COMPRESSION SCREW 1/2IN 47116202300 COMPRESSION SCREW 1-1/2IN 47116202200 COMPRESSION SCREW 1-1/4IN 47116202400 COMPRESSION SCREW 1-3/4IN 47116202100 COMPRESSION SCREW 1IN…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1147-2016·2016-03-23
Zimmer NexGen All-Poly Patella Components Recalled for Calibration Issues
Zimmer Manufacturing B.V. is recalling NexGen All-Poly Patella and related knee arthroplasty components due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.
Product
Product 49 consists of all product under product code: JWH and same usage: Item no: 597206529 NEXGEN ALL-POLY PATELLA, 597206532 NEXGEN ALL-POLY PATELLA, 597206535 NEXGEN ALL-POLY PATELLA, 597206538 NEXGEN ALL-POLY PATELLA, 597206541 NEXGEN ALL-POLY PATELLA, 598801713…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1102-2016·2016-03-23
Zimmer Manufacturing Recalls Sterile Bone Fixation Screws Due to Sealer Calibration
Zimmer Manufacturing B.V. is recalling 154 sterile bone fixation screws distributed nationwide due to insufficient sealer calibration data.
Product
Product 4 consists of all products under product code HWC, and same usage: Item no: 47482002603 2.0 X 26 CORT SCREW CRUCI 47482002803 2.0 X 28 CORT SCREW CRUCI 47482003203 2.0 X 32 CORT SCREW CRUCI 47482003403 2.0 X 34 CORT SCREW CRUCI 47482003603 2.0 X 36 CORT SCREW…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1112-2016·2016-03-23
Zimmer Manufacturing Recalls Sterile Intramedullary Fixation Rods Due to Calibration Issues
Zimmer Manufacturing B.V. is recalling sterile intramedullary fixation rods and lag screws due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.
Product
Product 14 consists of all product under product code HSB , and same usage: Item no: 225600230 ASIA ONE-PIECE LAG SCREW 225600232 ASIA ONE-PIECE LAG SCREW 225600235 ASIA ONE-PIECE LAG SCREW 225600237 ASIA ONE-PIECE LAG SCREW 225600240 ASIA ONE-PIECE LAG SCREW 225600242…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1139-2016·2016-03-23
Zimmer Manufacturing Recalls Sterile Bone Fixation Screws Due to Calibration Issues
Zimmer Manufacturing B.V. is recalling specific sterile bone fixation screws due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.
Product
Product 41 consists of all product under product code: KTT and same usage: Item no: 119301042 LAG SCR 12.7D X 100MM STA 119301045 LAG SCR 12.7D X 105MM STA 119301047 LAG SCR 12.7D X 110MM STA 119301050 LAG SCR 12.7D X 115MM STA 119301052 LAG SCR 12.7D X 120MM STA…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1132-2016·2016-03-23
Zimmer Manufacturing Recalls Sterile Knee Patella Components Due to Sealer Calibration
Zimmer Manufacturing B.V. is recalling 512 sterile I/B II Knee Domed Patella components for total knee arthroplasty due to insufficient sealer calibration data.
Product
Product 34 consists of all product under product code: JWH and same usage: Item no: 522001700 I/B II KNEE DOMED PATELLA 522001800 I/B II KNEE DOMED PATELLA 522001900 I/B II KNEE DOMED PATELLA for use in total knee arthroplasty
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1107-2016·2016-03-23
Zimmer Manufacturing Recalls Sterile Orthopedic Fixation Devices Due to Calibration Issues
Zimmer Manufacturing B.V. is recalling specific sterile orthopedic fixation devices due to insufficient sealer calibration data for products packaged between August 2010 and April 2013.
Product
Product 9 consists of all product under HRS, and same usage: Item no: 47494502601 4.5 BROAD SCP PLT, 26 HOL Product Usage: Temporary internal fixation devices designed to stabilize fractures during the normal healing process.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1156-2016·2016-03-23
Zimmer Manufacturing Recalls 119 Sterile Bone Fixation Appliances
Zimmer Manufacturing B.V. is recalling 119 sterile bone fixation appliances due to insufficient sealer calibration data. The affected products were packaged between August 2010 and April 2013.
Product
Product 58 consists of all product under product code: HRS and same usage: Item no: 234800904 PROXIMAL DORSAL ULNA PLT 234800906 PROXIMAL DORSAL ULNA PLT 234800908 PROXIMAL DORSAL ULNA PLT 234800910 PROXIMAL DORSAL ULNA PLT 234801004 PROXIMAL DORSAL ULNA PLT 234801006…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1123-2016·2016-03-23
Zimmer Manufacturing Recalls Distal Femoral Components for Sterility Concerns
Zimmer Manufacturing B.V. is recalling specific distal femoral components used in total hip arthroplasty due to insufficient sealer calibration data.
Product
Product 25 consists of all product under product code: LPH and same usage: Item no: 234703104 DISTAL MEDIAL FEMORAL CON 234703206 DISTAL MEDIAL FEMORAL CON 234703208 DISTAL MEDIAL FEMORAL CON 234800504 DISTAL POSTERIOR/LATERAL 234800506 DISTAL POSTERIOR/LATERAL 234800508…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1178-2016·2016-03-23
Teleflex Medical Recalls Pilling Modular Verres Body/Obturator Due to Packaging Error
Teleflex Medical is recalling 8 units of Pilling Modular Verres Body/Obturator (Product Code 140880) in Utah because customers were incorrectly provided with a different product code.
Product
Pilling Modular Verres Body/Obturator, Product Code 140880
Category
Medical Device
Distribution
1 state
LowFDA (Drugs)·D-0773-2016·2016-03-23
Teva Recalls Nabumetone Tablets Due to Missing Labels and Leaflets
Teva Pharmaceuticals USA is recalling 576 bottles of Nabumetone 750 mg tablets because they lack required leaflets and approved labels.
Product
NABUMETONE Tablets USP, 750 mg, 100 count bottle,Teva Pharmaceutical Industries Ltd., Jerusalem, 91010, ISRAEL
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0778-2016·2016-03-23
Pharmedium Recalls Subpotent Repinephrine Bitartrate Injection Bags
Pharmedium Services, LLC is recalling specific lots of repinephrine bitartrate injection bags due to subpotency and discoloration confirmed by FDA analysis.
Product
NORepinephrine Bitartrate, 8 mg (32 mcg/mL) added to 250 mL 0.9% Sodium Chloride Injection USP, in 250 mL Viaflex Bag Black, Rx only, PharMEDium Services, LLC, Sugar Land, TX NDC 61553-127-61
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·16V164000·2016-03-22
Forest River Recalls 2016 Cherokee Grey Wolf Trailers for Placard Error
Forest River is recalling 2016 Cherokee Grey Wolf recreational trailers because the Federal Placard lists incorrect tire and rim sizes, which may lead to overloading and tire blowouts.
Product
CHEROKEE — CHEROKEE GREY WOLF
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V165000·2016-03-22
Weiler Trucks Recalled for Missing Reflectors on LED Marker Lights
Weiler is recalling 368 trucks from 2002-2016 because LED marker lights lack required reflectors, reducing visibility and increasing crash risk.
Product
WEILER — WEILER B3, F1, F3, F5
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V163000·2016-03-21
Triumph Recalls 2016 Street Twin Motorcycles Due to Fuel Leak Fire Risk
Triumph is recalling 2016 Street Twin motorcycles because damaged wiring insulation may allow fuel to leak, increasing the risk of fire.
Product
TRIUMPH — TRIUMPH STREET TWIN
Category
Vehicle
Distribution
Distributed nationwide