State

Iowa product recalls

73,388 recalls have nationwide distribution and so reach Iowa. 5,590 additional recalls listed Iowa specifically in their distribution scope.

What the numbers show

Total: 5,590
Critical: 910
Severe: 1,590
Most recent: 2026-09-30

Of the 5,590 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 1,590 (28%) are Severe.

Which agencies issued them

These figures cover only the 5,590 recalls whose distribution notice names Iowa specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20526–20550 of 78978

HighFDA (Devices)·Z-1585-2022·2022-08-31
Medical Device Etching Solution Recalled for Potential Temperature-Related Effectiveness Loss
ABX Pentra Etching CP solution is recalled due to temperature excursions from June-August 2021 that may have affected product effectiveness. Affected lots were distributed June 1 - September 30, 2021.
Product
HORIBA ABX MEDICAL INC ABX PENTRA ETCHING CP System Fluid ABX Pentra Eching Solution CP For ABX Pentra 400 Clinical Chemistry Analyzer 25 mL. Ref: 1220001769
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1420-2022·2022-08-31
PREVACID Lansoprazole 15mg Capsules Recalled Due to Storage Conditions
Family Dollar Stores is recalling PREVACID 24HR Lansoprazole 15mg capsules distributed nationwide from April 30 to June 10, 2022, because the product was stored at improper temperatures in violation of manufacturing standards. Consumers should not use this product and should contact Family Dollar Stores for a refund.
Product
PREVACID 24HR LANSOPRAZOLE 15MG CAP 14CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1608-2022·2022-08-31
3M Grounding Safety Ring Pads Recalled Due to Temperature Exposure
3M Grounding Safety Ring pads may have been exposed to excessive temperatures during storage, potentially compromising product effectiveness. The recall affects products distributed nationwide that were received between June and September 2021.
Product
3M COMPANY 3M PAD, GROUNDING SAFETY RING Model Number: 9165
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1568-2022·2022-08-31
Enjoy Life Chewy Bars Recalled for Hard Plastic Contamination
Enjoy Life Natural Brands is recalling Chewy Bars - Caramel Blondie due to potential hard plastic pieces. About 89,736 cases were distributed in the US and Canada.
Product
Enjoy Life Chewy Bars Caramel Blondie (Chocolate Chip and Caramel), 5.75 oz (165g) UPC 819597011258 and 819597011333
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1568-2022·2022-08-31
Servo-air Ventilator Systems Lack Required Stability Warning Markings
Getinge is recalling Servo-air Ventilator Systems because they lack required warning markings about stability risks when stationary. A total of 102 units were distributed in the US; 13,750 units were distributed internationally.
Product
Servo-air Ventilator System-The Servo-air Ventilator System is: Intended for respiratory support, monitoring and treatment of pediatric and adult patients. Model Number: 6882000 (equipped with 6881999 mobile cart)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1586-2022·2022-08-31
ABX PENTRA Creatinine Reagent Recalled Due to Temperature Excursion Exposure
Mckesson Medical-Surgical is recalling ABX PENTRA Creatinine reagent due to facility temperature excursions (June-August 2021) that may have impacted product effectiveness. Affected lots were received nationwide between June 1 and September 30, 2021.
Product
a. ABX PENTRA CREATININE 120CP JAFFE 120/130. Ref: A11A01933. b. Reagent General Chemistry Creatinine Model Number: 1220001933
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1621-2022·2022-08-31
Medical Sponges Recalled for Temperature Exposure During Storage
Mckesson Medical-Surgical is recalling MetriSponge cleaning sponges due to facility temperature excursions that may have compromised product effectiveness during storage and delivery between June and August 2021.
Product
METREX RESEARCH CORP SPONGE, METRISPONGE W/METRIZYME (25/BX 4BX/CS) Model Number: 10-4025
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1606-2022·2022-08-31
Alere Fertility Test Pregnancy Test Kits Recalled Due to Temperature Damage
Alere Fertility Test pregnancy test kits distributed in the US have been recalled because temperature excursions during storage may have reduced product effectiveness. All lots received between June 1 and September 30, 2021 are affected.
Product
a. ABBOTT RAPID DX N AMERICA LLC Alere Rapid Test Kit Alere Fertility Test hCG Pregnancy Test Urine Sample 30 Tests, Model Number: 92210. b. ABBOTT RAPID DX N AMERICA LLC Alere Rapid Test Kit Alere hCG Dipstick Fertility Test hCG Pregnancy Test Urine Sample 50 Tests Model…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1628-2022·2022-08-31
Medical Lubricating Jelly Recalled Due to Temperature Excursions During Storage
Mckesson Medical-Surgical is recalling Fisher Scientific Aseptic Control Lubricating Jelly due to temperature excursions from June–August 2021 that may have reduced product effectiveness.
Product
FISHER SCIENTIFIC Aseptic Control¿ LUBRICATING JELLY PAP TEST 4OZ(12/PK) Catalog #22998006
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1402-2022·2022-08-31
Petroleum Jelly Products Recalled for Improper Storage Conditions
Family Dollar Stores is recalling three petroleum jelly products (Swan, Baby Love, and Vaseline brands) distributed between April and June 2022 due to storage temperature deviations.
Product
SWAN PETROLEUM JELLY 7.5 OZ SKU 910721 BABY LOVE PETROLEUM JELLY 13 OZ SKU 910726 VASELINE PETROLEUM JELLY ORIGINAL 7.5 OZ 2099273 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1398-2022·2022-08-31
AZO YEAST PLUS 20 CT Recalled Due to Improper Storage Conditions
AZO YEAST PLUS 20 CT has been recalled by Family Dollar Stores due to improper storage temperature conditions that violate CGMP requirements. The product was distributed nationwide from April through June 2022.
Product
AZO YEAST PLUS 20 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1584-2022·2022-08-31
Surgical Hemostatic Matrix Recalled Due to Temperature Exposure During Storage
Mckesson is recalling Ethicon SURGIFLO Hemostatic Matrix Kit due to temperature excursions during storage that may have reduced product effectiveness. Affected units were distributed nationwide between June and September 2021.
Product
Ethicon SURGIFLO Hemostatic Matrix Kit with Thrombin (6/CS) Ref: 2994 Mfg: FERROSAN MEDICAL DEVICES A/S Indicated in surgical procedures (other than ophthalmic) as an adjunct to hemostasis when control of bleeding by ligature or other conventional methods is ineffective…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1590-2022·2022-08-31
Alcon Contact Lens Solutions Recalled for Temperature Exposure During Storage and Transit
Multiple Alcon contact lens solutions were recalled due to facility temperature excursions during storage and transit that may have reduced product effectiveness. Affected products include Clear Care and Opti Free Replenish solutions distributed nationwide between June and September 2021.
Product
a. Alcon Clear Care Contact Lens Solution Clear Care 12 oz. Solution, Model Number: 65035820, Model Number: USSCupA-12BUP300. b. Alcon Contact Lens Solution Opti Free Replenish 4 oz. Solution Model Number: 00065035604 Model Number: USSCupA-12BUP300. c. Alcon Contact…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1595-2022·2022-08-31
Cadwell Disposable Ground Electrodes Recalled Due to Temperature Exposure
Cadwell Disposable Ground Electrodes may have reduced effectiveness due to facility temperature excursions between June and August 2021. All units distributed nationwide received between June 1 and September 30, 2021 are affected.
Product
Cadwell Disposable Ground Electrodes Grounding Pad 1.25 X 1.75 Inch Dimensions, Disposable Model Number: 302288-000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1580-2022·2022-08-31
Baxter Syringe Tip Caps Recalled Due to Sterile Packaging Barrier Risk
Baxter Healthcare is recalling DISCPAC Syringe Tip Caps because the packaging may not maintain a sterile barrier. The product was distributed nationwide and internationally.
Product
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Pink, 100 pack, REF H938676100
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1577-2022·2022-08-31
Baxter DISCPAC Syringe Tip Caps recalled for packaging sterility concerns
Baxter Healthcare is recalling DISCPAC Syringe Tip Caps due to potential packaging failures that could compromise the sterile barrier on 10,140 units distributed worldwide.
Product
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, White REF H938671100
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1444-2022·2022-08-31
AFRIN No Drip Severe Congestion Recalled for Improper Storage Temperature
Family Dollar Stores is recalling AFRIN No Drip Severe Congestion 0.5 FL oz due to improper storage temperature conditions (CGMP deviation). The product was distributed to specific Family Dollar locations from April 30 through June 10, 2022.
Product
AFRIN NO DRIP SEVERE CONGESTION 0.5FL OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·22V660000·2022-08-31
2022 Nissan Rogue Fuel Tank May Leak Following Modifications
Certain 2022 Nissan Rogue vehicles have fuel tanks that may have been punctured during vehicle modifications, creating potential fuel leak and fire risk. Nissan will inspect and replace affected fuel tanks free of charge.
Product
NISSAN — NISSAN redundant ROGUE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1615-2022·2022-08-31
MedSource IV Start Kit Recalled for Temperature-Related Effectiveness Loss
McKesson is recalling MedSource IV Start kits due to facility temperature excursions that may have compromised product effectiveness. Affected units were received between June and September 2021.
Product
MedSource IV Start kit, 8inch Extension Set IV START KIT, W/SITE LOC/8" EX100/CS Model Number: MS-80047
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1581-2022·2022-08-31
Baxter DISCPAC Syringe Tip Caps Recalled for Potential Sterile Barrier Failure
Baxter is recalling DISCPAC Syringe Tip Caps due to potential packaging defect that may not maintain sterile barrier. The recall affects 8,500 units distributed worldwide.
Product
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Purple, 100 pack, REF H938677100
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1366-2022·2022-08-31
Personal Care Lotions Recalled Due to Improper Storage Temperature
Family Dollar Stores is recalling multiple lotion products that were held outside appropriate storage temperatures. The affected brands include Dermasil, Aveeno, and Vaseline products distributed from April 30 through June 10, 2022.
Product
Dermasil Dry Skin Treatment 10 OZ SKU 2098068 Aveeno Daily Moisturizing Lotion 5 OZ SKU 2005444 Aveeno Baby Daily Moistue Lotion 8 OZ SKU 900016 Vaseline Mens Extra Strength Body and Face Lotion 10 OZ SKU 2003674 distributed to specific Family Dollar Stores 04/30/2022…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1410-2022·2022-08-31
Swan Povidone 4 FL OZ Recalled for Improper Storage Temperature
Family Dollar Stores recalled Swan Povidone 4 FL OZ due to storage temperature deviations that may affect product quality. Products distributed nationwide from April to June 2022 should not be used.
Product
SWAN POVIDONE 4 FL OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1436-2022·2022-08-31
Lidocaine Cream Products Recalled for Improper Storage Conditions at Family Dollar
Family Dollar is recalling Aspercreme with Lidocaine Creme (SKU 999852) and Icy Hot Lidocaine Cream (SKU 999853) distributed April 30 through June 10, 2022 nationwide due to improper storage temperature conditions.
Product
ASPERCREME WITH LIDOCAINE CREME 1.75 OZ SKU 999852 ICY HOT LIDOCAINE CREAM 1.75 OZ SKU 999853 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1409-2022·2022-08-31
Doctor Teal's Epsom Salt Recalled for Improper Storage Conditions
Family Dollar Stores is recalling Doctor Teal's Pure Epsom Salt packages distributed April 30–June 10, 2022 due to improper storage temperature conditions.
Product
DOCTOR TEALS PURE EPSOM SALT UNSCENTED 6 LBS SKU 999355 Ready in case EPSOM SALTS 2 LB SKU 909223 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1419-2022·2022-08-31
PEPCID antacid tablets recalled for improper storage temperature handling
Family Dollar Stores is recalling three PEPCID antacid products due to improper storage temperature conditions at specific Family Dollar locations from April through June 2022.
Product
PEPCID COMPLETE CHEWABLE TAB BERRY 8CT SKU 903365 PEPCID AC MAXIMUM STRENGTH TABLET 25 CT SKU 902063 PEPCID AC MAXIMUM STRENGTH TABLET 8 CT SKU 914773 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide