Recalls published in July 2026
Everything the FDA, USDA FSIS, CPSC and NHTSA announced in July 2026, newest first.
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Class II · 3 months ago
Medline medical convenience kits labeled as: 1) Total Joint Pack recall: Medline Industries, LP is issuing a recall for specific Medline convenience
Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low…
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Class II · 3 months ago
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters 5cc recall: Affected kits contain recalled Bard Silastic Foley Catheters. Catheters
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present…
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Class II · 3 months ago
Medline medical convenience kits labeled as: 1) Shoulder Pack recall: Medline Industries, LP is issuing a recall for specific Medline convenience
Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low…
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Class II · 3 months ago
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters 5cc recall: Affected kits contain recalled Bard Silastic Foley Catheters. Catheters
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present…
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Class II · 3 months ago
Ferno-Washington Inc Power F2 Powered Fastening System, Product No. 0567091 Powered recall: Product may experience accelerated roller wear and potential deformation
Product may experience accelerated roller wear and potential deformation due to interference between the roller assembly and rail. In the worst-case…
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Class II · 3 months ago
Boston Scientific Corporation Farastar Pulsed Field Ablation Generator recall: Labeling discrepancy: Devices distributed with Instructions For Use (IFU) did
Labeling discrepancy: Devices distributed with Instructions For Use (IFU) did not include FARAPOINT PFA catheter information.
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Class II · 3 months ago
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters 5cc recall: Affected kits contain recalled Bard Silastic Foley Catheters. Catheters
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present…
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Class II · 3 months ago
Karl Storz Endoscopy Flexible Hystero-Fiberscope Kits REF: 11264BBU1, 11264BBUK1 recall: Flexible hysteroscopes indicated for use during diagnostic and operative
Flexible hysteroscopes indicated for use during diagnostic and operative hysteroscopic procedures may contain an expired single use endoscopic seal…
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Class II · 3 months ago
ICU Medical Inc. Hotline Fluid Warming Set, single use device recall: ICU Medical became aware of an increased likelihood of leakage in specific
ICU Medical became aware of an increased likelihood of leakage in specific Lots of L-70 HOTLINE Fluid Warming Sets due to potentially inadequate…
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Class I · 3 months ago
Medline medical procedure convenience kit labeled as: 1) Total Knee-Lf recall: The procedure kits contain ICU Medical, Inc. pain management kits containing
The procedure kits contain ICU Medical, Inc. pain management kits containing Bupivacaine Hydrochloride in Dextrose Injection, USP, which were…
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Class II · 3 months ago
Boston Scientific Corporation Farastar Ablation Generator EU recall: Labeling discrepancy: Devices distributed with Instructions For Use (IFU) did
Labeling discrepancy: Devices distributed with Instructions For Use (IFU) did not include FARAPOINT PFA catheter information.
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Class II · 3 months ago
Medtronic MiniMed, Inc. MiniMed Go App, Model: MMT-8600 , MMT-8601 recall: For MiniMed Go app version 1.0.0 and 1.1.0, when the Set day and night
For MiniMed Go app version 1.0.0 and 1.1.0, when the Set day and night is turned OFF and missed dose or Correct high glucose alerts are enabled, the…
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Class II · 3 months ago
Alphatec Spine, Inc. SafeOp Patient Interface, REF: AIX11240, part of SafeOp 3: Neural recall: Intraoperative neuromonitoring device, due to a software issue
Intraoperative neuromonitoring device, due to a software issue, may experience loss or interruption of triggered electromyography (tEMG)…
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Class II · 3 months ago
Penumbra System RED 68 Reperfusion Catheter REF: RED68KIT recall: Due to manufacturing issues, reperfusion catheters may fractures
Due to manufacturing issues, reperfusion catheters may fractures
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Class II · 3 months ago
AVID Medical, Inc. Halyard Standard Line Insertion Pack. Model/ recall: Defects in the silicone seal, which may result in "doming" of the silicone
Defects in the silicone seal, which may result in "doming" of the silicone seal due to improper sealing, potentially leading to fluid occlusion or…
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Class II · 3 months ago
Boston Scientific Corporation Farastar Ablation Generator EU recall: Boston Scientific is replacing specific FARASTAR PFA generators which have
Boston Scientific is replacing specific FARASTAR PFA generators which have a configuration that is not compatible for use with the FARAPOINT PFA…
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Class II · 3 months ago
Boston Scientific Corporation Faradrive Steerable Sheath Clear recall: Boston Scientific's complaint investigations have identified that a subset
Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage…
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Class II · 3 months ago
Rohto-Mentholatum Co., Ltd. Rohto Cooling Eye Drops Dry Aid , Sterile recall: Lack of Assurance of Sterility
Lack of Assurance of Sterility
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Class II · 3 months ago
Major Pharmaceuticals Levothyroxine Sodium Tablets, USP, 150 mcg recall: Subpotent Drug
Subpotent Drug
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Class II · 3 months ago
Rohto-Mentholatum Co., Ltd. Rohto Cooling Eye Drops ALL-IN-ONE , Sterile 0.4 FL OZ recall: Lack of Assurance of Sterility
Lack of Assurance of Sterility
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Class III · 3 months ago
Ascend Laboratories, LLC Dabigatran etexilate Capsules, 110 mg, 60-count carton recall: Failed Impurities/Degradation Specifications: OOS result was observed during
Failed Impurities/Degradation Specifications: OOS result was observed during the related substance test analysis with respect to Impurity II…
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Class I · 3 months ago
JB Chemicals and Pharmaceuticals Ltd Cetirizine Hydrochloride Tablets USP 5 mg recall: Cross Contamination with Other Products: Customer complaints for appearance
Cross Contamination with Other Products: Customer complaints for appearance of discolored tablets and red dots observed on Cetirizine Hydrochloride…
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Class II · 3 months ago
Rising, Cyproheptadine Hydrochloride Syrup, 2mg/5 mL, 473 mL recall: Presence of Precipitate: medication was crystallizing and particles floating
Presence of Precipitate: medication was crystallizing and particles floating in the bottle
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Class II · 3 months ago
Major Pharmaceuticals Levothyroxine Sodium Tablets, USP, 50 mcg recall: Subpotent Drug
Subpotent Drug