State

Colorado product recalls

20,371 recalls have nationwide distribution and so reach Colorado. 0 additional recalls listed Colorado specifically in their distribution scope.

About recalls in Colorado

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Colorado consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

15451–15475 of 20371

HighFDA (Devices)·Z-1828-2022·2022-10-05
Coons Interventional Guidewire Recall Due to Packaging Sterility Breach
Cook Incorporated is recalling Coons Interventional Wire Guide devices because the chevron seal on packaging may be completely breached, compromising sterility. 1,236 units were distributed.
Product
Coons Interventional Wire Guide, Guidewire; Reference Part Number/GPN: THSF-35-145-COONS G02356 THSF-38-145-COONS G02324 THSF-35-180-COONS G02621 THSF-35-80-COONS G12268
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1761-2022·2022-10-05
NanoSight particle analyzer recalled for laser safety non-compliance
Malvern Panalytical is recalling approximately 111 NanoSight LM10 instruments with LM12 modules nationwide due to non-compliance with Class I laser safety requirements. Users may be exposed to unsafe laser radiation.
Product
NanoSight LM10 fitted with LM12 module. A laboratory instrument for determination of particle characteristics (e.g. size).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1762-2022·2022-10-05
Laboratory Instrument Recalled for Class 1 Laser Safety Non-Compliance
Malvern Panalytical is recalling 76 NanoSight LM10 laboratory instruments that do not comply with Class 1 laser safety requirements. The company is taking this action to prevent potential laser exposure risks.
Product
NanoSight LM10 fitted with LM14 module. A laboratory instrument for determination of particle characteristics (e.g. size).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1841-2022·2022-10-05
Roadrunner PC Wire Guide Recalled for Packaging Breach and Sterility Compromise
Cook Incorporated recalls Roadrunner PC Wire Guide devices due to packaging seal breaches that may compromise sterility. Devices were distributed nationwide and internationally.
Product
Roadrunner PC Wire Guide (The Firm), Guidewire Reference Part Number/GPN RPC-35-145 G06979 RPC-35-80 G09534
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V319000·2022-10-05
2022 Rivian R1T front passenger seat airbag may not deactivate for children
Certain 2022 Rivian R1T vehicles have a malfunctioning occupant classification system that fails to deactivate the front passenger airbag when a child or child seat is present, increasing injury risk during a crash.
Product
RIVIAN — 2022 RIVIAN R1T
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1547-2022·2022-10-05
Rifampin Capsules Recalled for Exceeding Impurity Specification Limits
Akorn, Inc. is recalling 18,145 bottles of Rifampin Capsules, USP 150 mg due to impurity levels exceeding the FDA's 5 ppm interim specification limit for 1-Methyl-4-Nitrosopiperazine (MNP).
Product
Rifampin Capsules, USP, 150 mg, 30-count bottle, Rx only, Distributed by: Akorn Operating Company, LLC, Gurnee, IL 60031, NDC 61748-015-30
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1806-2022·2022-10-05
Great Value Shredded Hash Browns Recalled for Listeria Contamination
Great Value Shredded Hash Browns are recalled due to potential Listeria monocytogenes contamination. Consumers should not consume the product.
Product
Item GV020, Great Value Shredded Hash Browns, 4 lbs. bag, 6/4 lbs. bags per case. Product is frozen and it's not ready to eat. Distributed By: Walmart Inc. Bentonville, AR 72716. UPC 0 78742 15557 9. Product contains Potatoes, Disodium Dihydrogen Pyrophosphate, Dextrose.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1857-2022·2022-10-05
Medline ClearPro Trach T-Piece Suction Catheter May Separate at Connector
Medline is recalling 136,080 ClearPro Trach T-Piece Closed Suction Catheters because the suction catheter can come apart from the connector during patient suctioning.
Product
MEDLINE CLEARPRO TRACH T-PIECE CLOSED SUCTION CATHETER, flat peel pouch EA, 10 EA per Inner Carton (IC), 20 EA/2 Inner cartons per Case (CS). Labeled as follows: a. TRACH T-PIECE, 14 Fr, Item Number/REF: DYNCPTP14; b. TRACH T-PIECE, 14 Fr, Item Number/REF: DYNCPTP14T
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1832-2022·2022-10-05
Cook Guidewire Products Recalled Due to Compromised Sterile Packaging
Cook Incorporated is recalling Fixed Core Wire Guide products due to potential breach of sterile packaging seals. Affected devices may have compromised sterility.
Product
Fixed Core Wire Guide, Guidewire Reference Part Number/GPN THSCF-25-180-3 G02165 TSCF-25-80-3 G00476
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1544-2022·2022-10-05
Oxytocin injection recalled for incorrect sodium chloride concentration
QuVa Pharma is recalling oxytocin injections due to incorrect formulation. Bags contain 0.45% sodium chloride instead of the intended 0.9%.
Product
oxyTOCIN 30 Units/500 mL (0.06 Units/mL) added to 0.9% Sodium Chloride, Injection for IV Use, High Alert, This is a Compounded Product for Institutional or Office Use Only, Not for Resale, QuVa PHARMA 519 Route 173, Bloomsbury, NJ 08804, Total volume: 500 mL bag, NDC: 70092-1068-
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1824-2022·2022-10-05
Cook guidewires recalled for compromised sterility due to packaging breach
Cook Incorporated is recalling Amplatz extra Stiff Wire Guides because packaging seals may be completely breached, potentially compromising device sterility.
Product
Amplatz extra Stiff Wire Guide, Stiff Guidewire (OUS ONLY); Reference Part Number: THSF-35-145-AES-SGH (GPN G06801) THSF-38-80-AES-SGH (GPN G06874)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1847-2022·2022-10-05
Medical Guidewire Recalled for Packaging Defect Affecting Sterility
Cook Incorporated is recalling Movable Core Wire Guide (Tefcor) guidewires due to a packaging defect where the chevron seal may be breached, potentially compromising device sterility.
Product
Movable Core Wire Guide (Tefcor), Guidewire (OUS ONLY) Reference Part Number/GPN TMT-35-145 G01677
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1842-2022·2022-10-05
Cook Rosen Curved Wire Guide Recall: Sterility Concerns
Cook Incorporated is recalling specific lots of Rosen Curved Wire Guide guidewires due to a complete breach of the packaging seal that may compromise device sterility. Affected devices were distributed nationwide in the US and worldwide.
Product
Rosen Curved Wire Guide, Guidewire Reference Part Number/GPN THSCF-35-220-1.5-ROSEN G01623 THSCF-35-80-1.5-ROSEN G01774 THSCF-35-180-1.5-ROSEN G01264 THSCF-35-145-1.5-ROSEN G01261
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1834-2022·2022-10-05
Cook Guidewire Devices Recalled for Packaging Defect and Sterility Compromise
Cook Incorporated is recalling fixed core wire guide devices due to packaging defects that may compromise device sterility. Approximately 5,669 units were distributed in the US and 5,286 internationally.
Product
Fixed Core Wire Guide (Straight), Guidewire Reference Part Number/GPN: C-SF-18-30 G02261 C-SF-25-40 G01937 TSF-18-260 G00590 C-SF-25-50 G01938 TSF-35-180 G00652 C-SF-18-40 G02255 TSF-25-145 G00617 TSF-32-145 G00638 C-SF-15-50 G02274 TSF-18-145 G00587 TSF-18-50 G00593
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1816-2022·2022-10-05
Siemens Magnesium Test Cartridges May Produce Erroneous Results Without Alert
Siemens Dimension Magnesium Flex reagent cartridges may produce inaccurate test results without triggering warning flags. Some results may show magnesium levels 15–59% lower than actual values.
Product
Dimension Magnesium (MG) Flex reagent cartridge Siemens Material Number (SMN)/REF (Catalog Number):10444963/DF57
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1836-2022·2022-10-05
Cook Newton Wire Guide Recalls Due to Potential Sterility Compromise
Cook Incorporated is recalling certain Newton Wire Guide surgical guidewires because packaging seals may be breached, potentially compromising device sterility.
Product
Newton Wire Guide (LT Taper/10cm Distal Flexibility), Guidewire Reference Part Number/GPN: TSFNA-35-145 G00701 TSCFNA-35-145-3 G00561
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1835-2022·2022-10-05
Cook Incorporated Recalls Guidewire Due to Packaging Seal Breach
Cook Incorporated is recalling Heavy Double Flexible Tipped Wire Guide devices due to potential packaging seal breach that may compromise sterility. Affected products were distributed domestically and worldwide.
Product
Heavy Double Flexible Tipped Wire Guide, Guidewire Reference Part Number/GPN: THDOC-35-60-0-3 G11949 C-HDOC-18-40-0-2 G09201 C-THDOC-18-40-0-2-HTS G26925
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1821-2022·2022-10-05
OSSUR Power Knee Prosthetics Recalled for Battery Dislodgement Risk
OSSUR Power Knee prosthetics are being recalled because the battery may dislodge from the device. Approximately 190 units are affected across the United States.
Product
OSSUR Power Knee REF PKA10003 OSSUR Power Knee REF PKA10003 OSSUR Power Knee REF PKA01001L OSSUR Power Knee REF PKA01001T
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1856-2022·2022-10-05
Medline suction catheters recalled due to connector separation risk
Medline ClearPro Trach Double Swivel Closed Suction Catheters may have the green connector separate from the device during patient suctioning. The recall affects 34,920 units distributed nationwide and internationally.
Product
MEDLINE CLEARPRO TRACH DOUBLE SWIVEL CLOSED SUCTION CATHETER, flat peel pouch EA, 10 EA per Inner Carton (IC), 20 EA/2 Inner cartons per Case (CS). Labeled as follows: a. TRACH DOUBLE SWIVEL, 12 Fr, Item Number/REF: DYNCPDS12T b. TRACH DOUBLE SWIVEL, 14 Fr, Item Number/REF:
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1820-2022·2022-10-05
Siemens IMMULITE Thyroid Test Kit Recalled for Falsely Low Results
Siemens is recalling IMMULITE 2000 and XPi Thyroid Stimulating Immunoglobulins test kits due to a -23% negative bias that may produce falsely low results, potentially delaying diagnosis of autoimmune thyroid disease.
Product
IMMULITE 2000 and IMMULITE 2000 XPi Thyroid Stimulating Immunoglobulins (TSI) Siemens Material Number (SMN): 10876421 US; 10713448 (OUS)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1546-2022·2022-10-05
Antidepressant Medication Recalled for Excessive Active Ingredient Potency
Leading Pharma, LLC is recalling Clomipramine Hydrochloride Capsules (25mg) with Lot B14221 due to testing that found 110.6% of the labeled active ingredient strength. The medication was distributed nationwide.
Product
CLOMIPRAMINE HYDROCHLORIDE — CLOMIPRAMINE HYDROCHLORIDE (CLOMIPRAMINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1845-2022·2022-10-05
Cook Lunderquist Ring Torque Wire Guide packaging breach may compromise sterility
Cook Incorporated is recalling Lunderquist Ring Torque Wire Guides due to a complete breach in the chevron seal of the packaging, which may compromise device sterility. The recall affects multiple lot numbers distributed nationwide and internationally.
Product
Lunderquist -Ring Torque Wire Guide, Guidewire Reference Part Number/GPN THSF-35-125-THG G27031 THSF-35-145-THG G27033
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1837-2022·2022-10-05
Cook Roadrunner PC Guidewires Recalled for Compromised Packaging Sterility
Cook Incorporated is recalling Roadrunner PC Hydrophilic Guidewires due to potential packaging seal breaches that may compromise device sterility. Affected devices were distributed in the United States and internationally.
Product
Roadrunner PC Hydrophilic Wire Guide, Hydrophilic Guidewire Reference Part Number/GPN: RPC-035145-0-5 G34131 RPC-035145 G18154 RPC-035145-5 G34132 RPC-038145-0-5 G34129 RFSPC-038145-0 G17539 RFSPC-035145 G17540 RPC-038145-0 G18155 RPC-035145-0 G18153 RFSPC-035145-0 G175
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1785-2022·2022-10-05
BD Pyxis MedBank Cabinet Software Update Prevents Drawer Access
A software update for BD Pyxis MedBank medication dispensing cabinets contains an incompatible file that prevents Matrix drawers from opening, potentially delaying medication access in healthcare facilities.
Product
BD Pyxis MedBank Cabinet Software v2.1.2.9 Legacy MedBank Cabinets with Matrix Drawers include: . CUBEX MedFlex operating with Windows 7 . MedBank 200 Main operating with Windows 7 . MedBank 500 Main operating with Windows 7. An automated dispensing cabinet intende
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1854-2022·2022-10-05
Barco Medical Network Adapter Recalled for Installation Issues
Barco NV recalls 169 NexxisOR system network adapters (models K9303078A and K9303097A) due to installation issues. The affected devices were distributed in Florida, Illinois, and New Jersey.
Product
Barco Medical Network Adapter, MNA-240, part of the NexxisOR system, Model Numbers: a) K9303078A, b) K9303097A
Category
Medical Device
Distribution
Distributed nationwide