State

Ohio product recalls

20,364 recalls have nationwide distribution and so reach Ohio. 0 additional recalls listed Ohio specifically in their distribution scope.

About recalls in Ohio

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 Ohio 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.

15601–15625 of 20364

HighFDA (Devices)·Z-1739-2022·2022-09-21
Isopure ACDS Hemodialysis Equipment Recalled for Electrical Shock Risk
Isopure Corp recalls its ACDS (Acidified Concentrate Distribution and Storage) system used in hemodialysis facilities due to a potential electrical safety hazard that may result in electric shock or arcing.
Product
Acidified Concentrate Distribution and Storage-The Isopure ACDS (Acidified Concentrate Distribution and Storage) with remote fill is intended to be used in Hemodialysis facilities for the storage and distribution of acid concentrate to be used in the treatment of Hemodialysis p
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1529-2022·2022-09-21
Injectable Medication TRI-MIX Recalled for Lack of Sterility Assurance
Carolina Infusion is recalling TRI-MIX 30/1/60 Injectable (5 ML vials) nationwide due to lack of assured sterility. The affected lots have Beyond Use Dates in August and September 2022. Contact your healthcare provider if you received this product.
Product
TRI-MIX 30/1/60 Injectable, 5 ML vial, Rx only, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1725-2022·2022-09-21
GXL Acetabular Hip Implant Liners Recalled Due to Packaging Defect
Exactech is recalling specific GXL acetabular hip implant liners due to non-conforming packaging that may cause accelerated device wear. The recall affects 1,017 devices distributed worldwide.
Product
GXL acetabular liners, orthopedic hip implant component. Product Line Numbers: a. 0 DEG ACUMATCH CONSTRAINED LINER SZ E 28MM ID, REF 144-28-05; b. 0 DEG ACUMATCH CONSTRAINED LINER SZ F 28MM ID, REF 144-28-06; c. 0 DEG ACUMATCH CONSTRAINED LINER SZ G 28MM ID, REF 144-28-07
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1718-2022·2022-09-21
Cook Roadrunner Hydrophilic Wire Guide Recalled for Potential Sterility Compromise
Cook Incorporated is recalling the Roadrunner UniGlide Hydrophilic Wire Guide due to failed packaging sterility testing. The device's sterility may be compromised.
Product
Roadrunner UniGlide Hydrophilic Wire Guide REFERENCE PART NUMBER (RPN): HPWS-35-80 ORDER NUMBER (GPN): G56151. For vascular catheter positioning and exchange in diagnostic and interventional procedures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1729-2022·2022-09-21
GXL Acetabular Liners Recalled Due to Non-Conforming Packaging
Exactech is recalling certain GXL acetabular liners packaged in non-conforming bags that may cause accelerated wear of the hip implant component. No injuries have been reported.
Product
GXL acetabular liners, orthopedic hip implant component. Product Line Numbers: a. NOVATION GXL LINER, NEUTRAL, 28MM ID, GROUP 1 CUPS, REF 130-28-51 b. NOVATION GXL LINER, NEUTRAL, 32MM ID, GROUP 2 CUPS, REF 130-32-52 c. NOVATION GXL LINER, NEUTRAL, 36MM ID, GROUP 3 CUPS, RE
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1733-2022·2022-09-21
GXL Hip Implant Liners Recalled for Packaging Defect Risk
Exactech is recalling specific GXL acetabular polyethylene hip implant liners because non-conforming packaging may cause accelerated wear. The company has distributed 4,956 affected devices worldwide.
Product
GXL acetabular liners, orthopedic hip implant component. Product Line Numbers: a. ALL POLYETHYLENE ACETABULAR CUP, CEMENTED 22MM SZ 42, REF 106-22-42; b. ALL POLYETHYLENE ACETABULAR CUP, CEMENTED 22MM SZ 44, REF 106-22-44; c. ALL POLYETHYLENE ACETABULAR CUP, CEMENTED 2
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1512-2022·2022-09-21
FDA Recalls Citroma Magnesium Citrate Laxative for Manufacturing Deviations
Vi-Jon is recalling Citroma magnesium citrate oral laxative due to Current Good Manufacturing Practice (CGMP) deviations. The recall affects units distributed nationwide and internationally.
Product
CITROMA — CITROMA (MAGNESIUM CITRATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1511-2022·2022-09-21
OTC Magnesium Citrate Laxative Recalled for Manufacturing Process Deviations
Magnesium citrate saline laxative products branded as CITROMA and multiple retail equivalents are subject to a Class II recall due to manufacturing process deviations. The voluntary recall affects millions of bottles distributed nationwide and internationally.
Product
CITROMA — CITROMA (MAGNESIUM CITRATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1513-2022·2022-09-21
Magnesium Citrate Saline Laxative Recalled for Manufacturing Deviations
Vi-Jon, LLC voluntarily recalled Magnesium Citrate Saline Laxative due to manufacturing process deviations. Over 8 million units of the product were distributed nationwide.
Product
Magnesium Citrate SALINE LAXATIVE, Oral Solution, 1.745 g, Grape Flavor, 10 FL OZ (296 mL), a) Best Choice UPC 0 70038 66220 4 Proudly Distributed By: Valu Merchandisers, Co. 5000 Kansas Ave Kansas City, KS 66106; b) CVS Health UPC 0 50428 30745 8 Distributed by: CVS Pharmacy,
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1741-2022·2022-09-21
PTS Panels CHOL+GLU Test Strips Recalled for Incorrect Instructions
PTS Panels CHOL+GLU Test Strips (lot A202) are recalled because incorrect instructions for use were packaged with the product. Distribution includes the US, Japan, and Russia.
Product
PTS Panels CHOL+GLU Test Strips (REF 1765)
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·22772·2022-09-15
Baby Trend Cityscape Travel Jogger Strollers Parking Brake Failure Recall
Baby Trend is recalling about 310 Cityscape Travel Jogger Strollers (Model TJ75B12A) because the parking brake can fail, creating a fall and injury risk for children. No injuries have been reported.
Product
Cityscape Travel Jogger Strollers, Model TJ75B12A
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·22222·2022-09-15
Cervélo R5 and Caledonia-5 Bicycles Recalled for Fall Hazard
Cervélo USA recalls about 1,800 Model Year 2022 R5 and Caledonia-5 bicycles and 182 ST31 LT replacement stems because handlebars can slip in the stem, causing loss of control and falls. One injury from a fall has been reported.
Product
Model Year 2022 Cervélo R5 and Caledonia-5 bicycles and Cervélo ST31 LT replacement stems
Category
Consumer Product
Distribution
Distributed nationwide
CriticalCPSC·22221·2022-09-14
ThyssenKrupp Residential Elevators Recalled Due to Child Entrapment Hazard
ThyssenKrupp Access Corp. is recalling about 16,800 residential elevators sold between 1996 and 2012 due to an entrapment hazard. Children can become trapped in the gap between exterior and interior doors, resulting in serious injury or death; one child death has been reported.
Product
thyssenkrupp Access Corp. Residential Elevators
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1476-2022·2022-09-14
Milk of Magnesia Recalled Nationwide for Microbial Contamination
Plastikon Healthcare LLC has recalled Milk of Magnesia USP nationwide due to microbial contamination in non-sterile products. The affected lot (20071A) included approximately 24,400 institutional-use cups.
Product
MILK OF MAGNESIA USP, 2400 mg/30 mL, Magnesium Hydroxide, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-6846-73.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1479-2022·2022-09-14
Antacid Oral Suspension Recalled Nationwide for Microbial Contamination
Plastikon Healthcare LLC is recalling an antacid oral suspension distributed nationwide due to microbial contamination. Affected lots 20051A (exp. Aug. 2022) and 20088A (exp. Sep. 2022) should not be used.
Product
Magnesium Hydroxide 2400 mg, Aluminum Hydroxide 2400 mg, Simethicone 240 mg MAX, per 30 mL Oral Suspension, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1478-2022·2022-09-14
Antacid Medication Recalled Nationwide for Microbial Contamination Risk
Plastikon Healthcare LLC is recalling 220,500 cups of antacid containing magnesium hydroxide and aluminum hydroxide due to microbial contamination.
Product
Magnesium Hydroxide 1200 mg, Aluminum Hydroxide 1200 mg, Simethicone 120 mg per 30 mL, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-6838-73
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1477-2022·2022-09-14
Milk of Magnesia USP Recalled for Microbial Contamination Nationwide
Plastikon Healthcare LLC is recalling Milk of Magnesia USP due to microbial contamination in non-sterile products. Lot 20074A, distributed nationwide for institutional use, should not be used.
Product
MILK OF MAGNESIA USP, 2400 mg/10 mL, Magnesium Hydroxide, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-6840-72.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1493-2022·2022-09-14
CORRECTDOSE Children's Pain Relief and Fever Reducer Acetaminophen Recalled for Manufacturing Control Violations
CORRECTDOSE Children's Fever Reducer (160 mg/5 mL acetaminophen) has been recalled due to manufacturing control deviations. The recall affects 1,464 units distributed nationwide.
Product
CORRECTDOSE Children's PAIN RELIEF & Fever Reducer, Cherry, (Acetaminophen 160 mg per 5 mL), 2.04 FL.OZ (60mL), packaged in 12-5mL individual doses, Distributed by Correct Dose Inc, Braintree MA 02184. NDC 62320-311-05 UPC 8 60003 67145 0
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1681-2022·2022-09-14
ChemoLock Infusion Ports Recalled for Unintended Disconnection Risk
ICU Medical recalls ChemoLock chemotherapy infusion ports for potential unintended disconnection due to spring variation, which may delay therapy and expose patients to caustic substances.
Product
Product Description/Item: ChemoLock Bag Spike, 10 units/CL-10-10; ChemoLock BAG SPIKE w/ ADDITIVE PORT, DRY SPIKE/CL-12; APPX 1.5ml,ChemoLock BAG SPIKE WITH ADDITIVE PORT/CL-13; ChemoLock Port/CL2100; ChemoLock Port, 5 Units/CL2100-5; ChemoLock Port/CL2100T; Clave Bag Spike
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1686-2022·2022-09-14
King's Hawaiian Pretzel Buns Recalled for Potential Bacterial Contamination
King's Hawaiian pretzel hamburger buns, slider buns, and pretzel bites are recalled nationwide. An ingredient used in manufacturing may contain Cronobacter sakazakii or Clostridium botulinum.
Product
King's Hawaiian 10.5 oz. Pretzel Hamburger Buns (UPC 73435000365), 10.2 oz. Pretzel Bites (UPC 73435000525.), and 11 oz. Slider Buns (UPC 73435000372 ) packed in plastic bags. Distributed by King s Hawaiian Bakery West, Inc., 19161 Harborgate Way, Torrance, CA 90501
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1499-2022·2022-09-14
Difluprednate Eye Drops Recalled for Defective Container Sterility Risk
Cipla is recalling 117,844 bottles of Difluprednate eye drops nationwide due to defective containers where the protective cap can break, potentially exposing the dropper tip and compromising sterility.
Product
DIFLUPREDNATE — DIFLUPREDNATE (DIFLUPREDNATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1677-2022·2022-09-14
CARTO VIZIGO Guiding Sheath Recalled Due to Water-Damaged Sterile Packaging
Biosense Webster is recalling 98 units of CARTO VIZIGO 8.5F guiding sheaths due to water damage to packaging that may have compromised the sterile barrier, creating a potential infection risk.
Product
CARTO VIZIGO 8.5F Bi-Directional Guiding Sheath, REF: D138501. Used to introduce various cardiovascular catheters into the heart.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1678-2022·2022-09-14
External Fixation Wire May Fracture During Surgery, Leaving Fragments in Patient
OrthoPediatrics Corp is recalling an external fixation wire due to manufacturing variance that may cause the tip to fracture. Fractured fragments could remain in patients.
Product
Orthex External Fixation Wire Sharp Bayonet 1.8 x 400 mm Model: K400-18BN
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1684-2022·2022-09-14
Early Bird Bleed Monitoring System Introducer fails to power on
Saranas, Inc. is recalling 953 units of the Early Bird Bleed Monitoring System Introducer Sheath Set due to a design error that prevents the device from powering on and completing self-tests. The product was distributed nationwide.
Product
Early Bird Bleed Monitoring System Introducer Sheath Set, REF: FG001-01 (6F), FG001-02 (8F)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1495-2022·2022-09-14
Lidocaine Hydrochloride Jelly Recalled Due to cGMP Deviations and Turbidity
Akorn, Inc. is recalling 82,689 tubes of Lidocaine Hydrochloride Jelly USP, 2%, due to cGMP deviations and turbidity discovered during sterility testing. The recall affects multiple lots distributed nationwide.
Product
Lidocaine Hydrochloride Jelly USP, 2%, Sterile, 30mL tube, Rx only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-711-31
Category
Drug
Distribution
Distributed nationwide