State

Iowa product recalls

73,566 recalls have nationwide distribution and so reach Iowa. 5,593 additional recalls listed Iowa specifically in their distribution scope.

What the numbers show

Total: 5,593
Critical: 910
Severe: 1,591
Most recent: 2026-10-24

Of the 5,593 recalls naming Iowa we have scored against our rubric, 910 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,591 (28%) are Severe.

Which agencies issued them

These figures cover only the 5,593 recalls whose distribution notice names Iowa specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25201–25225 of 79159

ModerateFDA (Drugs)·D-0835-2021·2021-10-06
Neutrogena COOLDRY SPORT Sunscreen Spray Class II Recall
Johnson & Johnson Consumer, Inc. is recalling 678,384 cans of Neutrogena COOLDRY SPORT sunscreen spray nationwide due to current Good Manufacturing Practice (cGMP) deviations.
Product
Neutrogena COOLDRY SPORT sunscreen spray BROAD SPECTRUM SPF 70, Avobenzone (3%), Homosalate (15%), Octisalate (5%), Octocrylene (10%), NET WT. 5.0 OZ (141 g) aerosol can, Distributed by: JOHNSON & JOHNSON CONSUMER, INC. Skillman, NY 08858, UPC 0 86800 10037 9
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0842-2021·2021-10-06
Neutrogena COOLDRY SPORT Sunscreen Spray Recalled for cGMP Deviations
Johnson & Johnson Consumer, Inc. is recalling Neutrogena COOLDRY SPORT WITH MICROMESH SUNSCREEN SPRAY (5.5 oz, SPF 50) due to cGMP (current Good Manufacturing Practice) deviations. Approximately 1.4 million cans distributed nationwide are affected.
Product
Neutrogena COOLDRY SPORT WITH MICROMESH SUNSCREEN SPRAY Broad Spectrum SPF 50, Avobenzone 2.7%, Homosalate 5%, Octisalate 4.5%, Octocrylene 6%, Oxybenzone 4.5%. NET WT. 5.5 OZ. (155 g) aerosol can, Distributed by: JOHNSON & JOHNSON CONSUMER, INC. Skillman, NJ 08858, UPC 0 86800…
Category
Drug
Distribution
Distributed nationwide
ModerateCPSC·22004·2021-10-06
Hobby Lobby White Wood Stools Recalled for Fall and Injury Hazards
Hobby Lobby is recalling about 14,000 White Wood Stools sold nationwide from June through July 2021 because the stools can break during use, posing fall and injury hazards. Hobby Lobby has received seven reports of the stool breaking, including six resulting in minor injuries.
Product
White Wood Stools
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0832-2021·2021-10-06
Neutrogena COOLDRY SPORT Sunscreen Spray Recalled for cGMP Deviations
Johnson & Johnson is recalling Neutrogena COOLDRY SPORT sunscreen spray SPF 30 in two sizes nationwide due to cGMP (current Good Manufacturing Practice) deviations. The recall affects approximately 469,764 cans.
Product
Neutrogena COOLDRY SPORT sunscreen spray SPF 30, Avobenzone (3%), Homosalate (8%), Octisalate (5%), Octocrylene (8%), a) Net Wt 5.0 oz (141g) (UPC 0 86800 10035 5) and b) Net Wt. 8 oz. (226 g) UPC 0 86800 10031 7 aerosol can, Distributed by: JOHNSON & JOHNSON CONSUMER INC.…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0833-2021·2021-10-06
Neutrogena Beach Defense Sunscreen Spray Recalled for cGMP Deviations
Johnson & Johnson Consumer is recalling Neutrogena Beach Defense water + sun protection sunscreen spray in two sizes (6.5 oz and 8.5 oz) nationwide due to current good manufacturing practice (cGMP) deviations.
Product
Neutrogena Beach Defense water + sun protection sunscreen spray BROAD SPECTRUM SPF 30, Avobenzone (3%), Homosalate (8%), Octisalate (5%), Octocrylene (8%), a) NET WT. 6.5 OZ (184 g) (UPC 0 86800 87273 3) and b) NET WT. 8.5 oz (240 g) (UPC 0 86800 10032 4) aerosol can…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0854-2021·2021-10-06
Valproic Acid Oral Solution Recalled for Microbial Contamination
American Health Packaging is recalling Valproic Acid Oral Solution due to potential microbial contamination in liquid sugar batches used during manufacturing. The affected product was distributed nationwide.
Product
Valproic Acid Oral Solution, USP, 500 mg/10 mL, 100 10 mL unit dose cups per case, Rx Only, Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217 Case NDC#: 60687-262-56; Individual Dose NDC: 60687-262-42
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0869-2021·2021-10-06
Viola Odorata Homeopathic Medicine Recall for Failed Identification Testing
Washington Homeopathic Products is recalling Viola Odorata homeopathic medicine (Lot #29057, expiration 8/17/2026) distributed nationwide because identification testing using HPTLC analysis returned out-of-specification results.
Product
Viola Odorata 4X, 10X, 12X, Bee Stings*, Sucrose/Lactose Pills, 4X Packaged in a) 2 Dram; 10X Packaged in b) 2 Dram; 12X Packaged in c) 2 Dram; d) 4 Dram; WHP Homeopathic Medicine, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV, 25411.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2568-2021·2021-10-06
Olympus BF-P60 Bronchofiberscope Reprocessing Instructions Updated to Meet FDA Guidance
Olympus Corporation has issued new, validated reprocessing instructions for the BF-P60 OES Bronchofiberscope to comply with FDA guidance. The recall affects 1,030 devices distributed nationwide and internationally.
Product
BF-P60 OES Bronchofiberscope, Model No. BF-P60
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0881-2021·2021-10-06
ZTE-1020 Homeopathic Formula Recalled for Failed Identification Testing
Washington Homeopathic Products, Inc. is recalling ZTE-1020 Formula (1000ml bottle, Lot #25740) distributed nationwide because identification testing based on HPTLC analysis produced out-of-specification results.
Product
ZTE-1020 Formula. Contents 1000ml. WHP Homeopathic Medicine, For Manufacturing Use Only, REMEDY: Aurum Metallicum 10X, Crataegus Oxyacantha 10X, Baryta Carbonica 10X, Digitalis Purpurea 10X, Zincum Muriaticum 13X, Chromium Sulphuricum 10X, Manganum Metallicum 10X, Dilution…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0858-2021·2021-10-06
ZTE-105 Formula Gentle Detoxing Recall Due to Failed Identification Testing
Washington Homeopathic Products is recalling ZTE-105 Formula Gentle Detoxing due to out-of-specification test results from identification testing. The product was distributed nationwide.
Product
ZTE-105 Formula Gentle Detoxing. Contents 1000 mL, RX Only, REMEDY: Bryoni Alba 10X, Chelidonium Majus 10X, Carduus Marianus 10X, Dolichos Pruriens 10X, Solidago Vigaurea 10X, Alfalfa 10X, Boldo 10X, Cynara Scolymus 10X, Zincum Muriaticum 13X, Chromium Sulphuricum 10X, Manganum…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0849-2021·2021-10-06
Neutrogena Beach Defense Sunscreen Spray Recalled for cGMP Deviations
Johnson & Johnson Consumer, Inc. is recalling Neutrogena Beach Defense water+sun protection sunscreen spray (SPF 50, 6.5 oz aerosol) distributed nationwide due to current good manufacturing practice (cGMP) deviations. The recall is voluntary and initiated by the firm.
Product
Neutrogena Beach Defense water+sun protection sunscreen spray BROAD SPECTRUM SPF 50, Avobenzone (3%), Homosalate (10%), Octisalate (5%), Octocrylene (10%), NET WT. 6.5 OZ. (184 g) aerosol can, Distributed by: JOHNSON & JOHNSON CONSUMER, INC. Skillman, NJ 08858, UPC 0 86800 11254…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0883-2021·2021-10-06
Z-1050 Formula Hepatodetox Homeopathic Medicine Fails Identification Testing
Washington Homeopathic Products, Inc. is recalling Z-1050 Formula Hepatodetox 1000ml bottles because out-of-specification test results were obtained during identification testing based on HPTLC analysis.
Product
Z-1050 Formula Hepatodetox. Contents 1000ml. WHP Homeopathic Medicine, For Manufacturing Use Only, REMEDY: Cholesterinum 10X, Avena Sativa 12X, Cynara Scolymos 12X, Phosphorus 12X, Oroticum Acidum 13X, Aesculus Hipposcastanum 24X, Carduus Marianus 24X, Chelidonium Majus 24X…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0862-2021·2021-10-06
Cedar Fever Drops Homeopathic Drug Recalled for Failed Identification Testing
Washington Homeopathic Products is recalling Cedar Fever Drops due to out-of-specification test results from identification testing. The affected product was distributed nationwide.
Product
Cedar Fever Drops, 20% USP ALCOHOL, 30 mL, homeopathic drug for symptoms of cder allerges, Manufactured for Peoples RX, 3801 S Lamar, Austin, TX 78704. UPC 7 40640 64166 8
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2570-2021·2021-10-06
Olympus BF-XT160 Bronchovideoscope Reprocessing Instructions Updated for FDA Compliance
Olympus Corporation is issuing updated reprocessing instructions for 293 BF-XT160 bronchovideoscopes to comply with FDA 2015 guidance. Healthcare facilities should implement the new sterilization and disinfection procedures.
Product
BF-XT160 EVIS EXERA Bronchovideoscope, Model No. BF-XT160
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0837-2021·2021-10-06
Neutrogena Ultra Sheer Sunscreen Body Mist Recalled for cGMP Deviations
Johnson & Johnson Consumer is recalling Neutrogena Ultra Sheer body mist sunscreen in 5 oz and 8 oz aerosol cans nationwide due to current good manufacturing practice (cGMP) deviations. The recall is voluntary and initiated by the firm.
Product
Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 45, Avobenzone (3%), Homosalate (10%), Octisalate (5%), Octocrylene (10%), a) Net Wt. 5 OZ (141 g) (UPC 0 86800 10039 3) and b) Net Wt. 8.0 oz. (226 g) (UPC 0 86800 11134 4) aerosol can, Distributed by: JOHNSON &…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0894-2021·2021-10-06
Aconitum nap Fear Homeopathic Medicine Recalled for Failed Product Identification Testing
Washington Homeopathic Products is recalling Aconitum nap Fear 20% Alcohol homeopathic medicine (Lot #26198) distributed nationwide due to out-of-specification test results from HPTLC identification analysis.
Product
Aconitum nap Fear* 20% Alcohol HPUS: 6X, packaged in 50mL & 8 oz containers Aconitum nap Fear* 20% Alcohol HPUS: 7X, 12X, packaged in 15mL containers WHP Homeopathic Medicine, Washington Homeopathic Products 260 JR Hawvermale Way, Berkeley Springs, WV 25411.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0884-2021·2021-10-06
Z-1070 Formula Anxioheal Homeopathic Medicine Recall for Testing
Washington Homeopathic Products, Inc. is recalling Z-1070 Formula Anxioheal, a 1000ml homeopathic remedy containing 20% alcohol, due to out-of-specification test results from HPTLC identification testing. The product was distributed nationwide.
Product
Z-1070 Formula Anxioheal. Contents 1000ml 20% Alcohol. WHP Homeopathic Medicine, For Manufacturing Use Only, REMEDY:Causticum 30X, Conium Maculatum 8X, Conium Maculatum 12X, Crataegus Oxyacantha 12X, Crataegus Oxyacantha 30X, Ignatia Amara 24X, Lycopus Virginicus 12X…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0859-2021·2021-10-06
Washington Homeopathic Products Occular Allergy Blend fails identification testing
Washington Homeopathic Products is recalling Occular Allergy Blend 87% Alcohol (Lot # 30148, 500 mL bottles) distributed nationwide due to out-of-specification test results in identification testing.
Product
Occular Allergy Blend 87% Alcohol; In Equal Parts of Apis Mellifica 7x Allium Cepa 7x Euphrasia Officinalis 7X Sabadilla 7X, WHP Homeopathic Medicine For Manufacturing Only, 500 ml. Manufcatured by Washington Homeopathic Products 260JR Hawvermale Way, Berkeley Springs WV 25411
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0893-2021·2021-10-06
Aconitum Napellus Fear Pills Recalled for Failed Quality Testing
Washington Homeopathic Products is recalling Aconitum Napellus Fear homeopathic pills in multiple potencies and package sizes (562 bottles, Lot #26198) distributed nationwide because test results showed out-of-specification identification results on HPTLC analysis.
Product
Aconitum Napellus Fear* Sucrose/Lactose Pills HPUS: 8X, 9X, 12X,30X, packaged in 1 oz containers, Aconitum Napellus Fear* Sucrose/Lactose Pills HPUS: 6X, 10X, 15X, 24X, 30X, packaged in 2 dr containers, Aconitum Napellus Fear* Sucrose/Lactose Pills HPUS: 6X, 30X, packaged in 2…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0865-2021·2021-10-06
Washington Homeopathic Cistus Canadensis pills fail quality identification testing
Washington Homeopathic Products is recalling Cistus Canadensis homeopathic pills in multiple potencies because they failed out-of-specification identification testing. The recall affects 17 bottles distributed nationwide.
Product
Cistus Canadensis 6X, 10X, 15X, 30X, Coldness* Sucrose/Lactose Pills, 6X Packaged as a) 1 OZ, UPC 7 40640 28177 2, b) 4 dr, UPC 7 40640 28173 4; 10X Packaged as c) 4 dr; 15X Packaged as d) 1 OZ; 30X Packaged as e) 2 Dram, UPC 7 40640 28171 0, f) 4 dr, UPC 7 40640 28175 8; WHP…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0851-2021·2021-10-06
Lyrica CR 330 mg Tablets Recalled for Failed Dissolution
Viatris is recalling Lyrica CR (pregabalin) 330 mg extended-release tablets nationwide due to failed dissolution specifications that may reduce drug effectiveness.
Product
Lyrica CR (pregabalin) extended release tablets, 330 mg, 30-count bottles, Rx only, Distributed by Parke-Davis Division of Pfizer Inc., NY, NY 10017, NDC 0071-1029-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0871-2021·2021-10-06
Washington Homeopathic Products Kali Sulphuricum fails identification test
Washington Homeopathic Products is recalling Kali Sulphuricum 3X homeopathic medicine nationwide because identification testing using HPTLC analysis produced out-of-specification results.
Product
Kali Sulphuricum 3X, 960ml 20% Alcohol, WHP Homeopathic Medicine, For Manufacturing Use Only. Manufactured by Washington Homeopathic Products 260JR hawvermale Way Berkeley Springs WV 25411.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0841-2021·2021-10-06
Neutrogena Beach Defense SPF 100 sunscreen spray recalled for cGMP deviations
Johnson & Johnson is recalling Neutrogena Beach Defense water+sun protection sunscreen spray (SPF 100, 6.5 oz aerosol cans) nationwide due to cGMP manufacturing deviations. The recall was voluntarily initiated by the company.
Product
Neutrogena Beach Defense water+sun protection sunscreen spray BROAD SPECTRUM SPF 100, Avobenzone (3%), Homosalate (15%), Octisalate (5%), Octocrylene (10%), Oxybenzone (6%), NET WT. 6.5 OZ (184 g) aerosol can, Distributed by: JOHNSON & JOHNSON CONSUMER, INC. Skillman, NJ 08858…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0898-2021·2021-10-06
Sodium Phenylbutyrate Powder Recalled for Impurity Specification Failures
SigmaPharm Laboratories is recalling Sodium Phenylbutyrate Powder due to failed impurity and degradation specifications detected during routine testing. The affected lots are distributed nationwide.
Product
Sodium Phenylbutyrate Powder, 250 Grams, Rx Only, packaged in 500 cc HDPE bottles and 53 mm CRC caps packed in a carton and then in case packs containing 2 bottles. Sigmapharm Laboratories, LLC, Bensalem, PA 19020, NDC 42794-086-14
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0831-2021·2021-10-06
Aveeno Protect + Refresh Sunscreen Spray Recalled for cGMP Deviations
Johnson & Johnson Consumer, Inc. is recalling Aveeno Protect + Refresh sunscreen weightless spray SPF 60 nationwide due to cGMP (current good manufacturing practice) deviations.
Product
Aveeno Protect + Refresh sunscreen weightless spray with oat SPF 60, Avobenzone (3%), Homosalate (10%), Octisalate (5%), Octocrylene (10%), NET WT. 5.0 (OZ) (141 g) aerosol can, Distributed by: Johnson & Johnson Consumer Inc., Skillman, NJ 08558 UPC 3 8137-119462 9
Category
Drug
Distribution
Distributed nationwide