State

Puerto Rico product recalls

72,940 recalls have nationwide distribution and so reach Puerto Rico. 3,090 additional recalls listed Puerto Rico specifically in their distribution scope.

What the numbers show

Total: 3,090
Critical: 366
Severe: 625
Most recent: 2026-09-02

Of the 3,090 recalls naming Puerto Rico we have scored against our rubric, 366 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 625 (20%) are Severe.

Which agencies issued them

These figures cover only the 3,090 recalls whose distribution notice names Puerto Rico specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4151–4175 of 76030

HighFDA (Devices)·Z-0601-2026·2025-12-03
Brain access devices recalled because packaging tape contains latex
Stryker is recalling 39,148 NICO BrainPath devices because tape used to secure components in the packaging contains latex despite the products being labelled latex-free.
Product
NICO BrainPath; Product Number/Product Name NN-8024 BrainPath Shephard's Hook - Greenberg; NN-8025 BrainPath Shephard's Hook - Sugita; NN-8026 BrainPath Shephard's Hook - Budde; NN-8042 BrainPath Shephard's Hook - Greenberg LK;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0723-2026·2025-12-03
Imaging software recalled over a bug that can lose clinical information
Intelerad Medical Systems is recalling 19 IntelePACS InteleConnect and TechPortal installations because a bug can cause data loss in the Relevant Clinical Info field.
Product
IntelePACS - InteleConnect / TechPortal
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0720-2026·2025-12-03
Anesthesia vaporizers recalled over the potential for anesthesia leakage
Mindray is recalling 148 Sevoflurane V90 Electronic Vaporizers used with the A9 Anesthesia System over the potential for anesthesia leakage.
Product
Sevoflurane (SEVO) V90 Electronic Vaporizer with the A9 Anesthesia System. Labeled as the following: 1. Sev E_Vap. (Safety Filling adapter), Part Number: 115-066756-00. 2. Exchange Sev E_Vap. (Safety Filling adapter), Part Number: E115-066756-00. Product Description: Th
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0594-2026·2025-12-03
Diabetes clinic software recalled over incorrect sensor glucose graph data
Medtronic MiniMed is recalling 12,126 CareLink Clinic installations because a software error displays incorrect data on the 24-hour sensor glucose overview graph.
Product
CareLink Clinic, REF: MMT-7350
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0599-2026·2025-12-03
Myriad handpieces recalled because packaging tape contains undisclosed latex
Stryker is recalling 39,148 NICO Myriad Handpieces because tape used to secure components in the packaging contains latex despite the products being labelled latex-free.
Product
NICO Myriad Handpiece Product Number/Product Name: NN-8000 15x10 MHP; NN-8001 15x 13 MHP; NN-8002 15x 25 MHP - MINOP; NN-8003 13x10 MHP; NN-8004 13x13 MHP; NN-8005 15x25 MHP GAAB; NN-8006 11X10 MHP; NN-8007 11x13 MHP; NN-8008 19x28 MHP OI; NN-8010 17x31.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0588-2026·2025-12-03
Heated massage tables recalled over heat components that can smolder
Pivotal Health Solutions is recalling 464 Quantum Intersegmental Tables because damage to the heat function components can lead to overheating, smoldering and melting of the vinyl cushion.
Product
Quantum Intersegmental Table, Model/Catalog Number: AMQ400H; heated massage table
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0582-2026·2025-12-03
Demonstration only gel recalled because it may be placed in patients
Straumann USA is recalling 61 units of Emdogain because product intended for demonstration purposes only could be placed in patients.
Product
Emdogain; Article Numbers: (1) 440.230V10, (2) 475.132V10;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0578-2026·2025-12-03
IV set 490487 recalled over piggyback backflow and occlusion risk
B. Braun Medical is recalling 23,160 units iv administration sets over the potential for medication backflow from secondary piggyback containers and an inability to prime.
Product
FoundationOne Liquid CDx (F1LCDx), TECH-0009 version 6.0
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V836000·2025-12-03
Volkswagen ID.4 recalled for high-voltage battery fire risk
Volkswagen is recalling approximately 629 2023-2024 ID.4 vehicles with defective high-voltage battery cell modules. Misaligned electrodes in the battery may cause fires, posing a risk of injury to vehicle occupants.
Product
VOLKSWAGEN — VOLKSWAGEN ID.4
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0179-2026·2025-12-03
Saline nasal spray recalled over microbial contamination with Pseudomonas lactis
Medical Products Laboratories is recalling 41,328 bottles of Walgreens Saline Nasal Spray with Xylitol over microbial contamination identified as Pseudomonas lactis.
Product
Walgreens Saline Nasal Spray WITH XYLITOL, 1.5 oz (45mL) bottle, DISTRIBUTED BY: WALGREEN CO., 200 WILMOT RD., DEERFIELD, IL 60015, NDC 0363-3114-01
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·25V835000·2025-12-03
2026 Volkswagen ID.4 and Atlas vehicles recalled for incorrect wheel bolts
Volkswagen is recalling 27 vehicles with potentially incorrect wheel bolts that could detach during driving. Owners should not drive their vehicles until bolts are inspected and replaced by a dealer at no cost.
Product
VOLKSWAGEN — VOLKSWAGEN ID.4, ATLAS CROSS SPORT, ATLAS
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0183-2026·2025-12-03
Schwab mineral sunscreen recalled over manufacturing practice deviations at Botana
CA Botana International is recalling 1,167 tubes of Doctor D. Schwab Mineral Sunscreen SPF 50 for CGMP deviations.
Product
Doctor. D. Schwab Mineral Sunscreen SPF 50, Zinc Oxide 21%, 4 oz./ 113.4 g per tube, Manufactured by CA Botana, San Diego, CA 92123. NDC: 35192-042-02
Category
Drug
Distribution
5 states
ModerateFDA (Devices)·Z-0585-2026·2025-12-03
Culture media recalled over contamination that may darken the broth
Remel is recalling cation-adjusted Mueller Hinton broth and Brucella broth because the products may contain contamination, which may result in a darker or brown media color.
Product
1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0187-2026·2025-12-03
Mineral sunscreen recalled over current good manufacturing practice deviations
CA Botana International is recalling 874 tubes of Sea Enzyme Ultra Umbrella Sunscreen SPF 30 for CGMP deviations.
Product
Sea Enzyme Ultra Umbrella Sunscreen SPF 30, Titanium Dioxide 4%, Octinoxate 4%, 4 oz./113.4 g per tube, Manufactured by CA BOTANA, San Diego, CA 92121. NDC: 35192-011-02
Category
Drug
Distribution
5 states
ModerateFDA (Drugs)·D-0196-2026·2025-12-03
Menthol pain relief gel recalled over manufacturing practice deviations
CA Botana International is recalling 4,890 bottles of Dr. Bump Natural Pain Relief Gel with Menthol 5% for CGMP deviations.
Product
Dr. Bump Natural Pain Relief Gel, Menthol 5%, NET WT 4 FL OZ/118 ML per bottle, Distr. by 1Beauty US LLC, Palm Desert, CA 92211. NDC: 35192-052-18, UPC 8 18204 02513 8
Category
Drug
Distribution
5 states
ModerateFDA (Devices)·Z-0577-2026·2025-12-03
Cancer test reports recalled for omitting the companion diagnostic claims page
Foundation Medicine is recalling 59 FoundationOne CDx reports that were sent to customers without the companion diagnostic Claims Page.
Product
FoundationOne CDx (F1CDx), RAL-0003 version 31.0
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0191-2026·2025-12-03
Daily moisturizer recalled over current good manufacturing practice deviations
CA Botana International is recalling 1,492 tubes of Karina Daily Moisturizer SPF 25 for CGMP deviations.
Product
Karina Daily Moisturizer SPF 25, Octinoxate 7.5% and Zinc Oxide 7.0%, Net WT. 5 oz/ 141.7 g per tube, Dist. By: Beauty4Pros LLC, Palm Desert, CA 92211. NDC: 35192-033-16, UPC 8 18204 02572 5
Category
Drug
Distribution
5 states
ModerateFDA (Drugs)·D-0194-2026·2025-12-03
Elixir tinted sunscreen recalled over manufacturing practice deviations
CA Botana International is recalling Elixir by Coco March Tinted Mineral Sunscreen SPF 50 for CGMP deviations.
Product
Elixir by Coco March Tinted Mineral Sunscreen SPF 50, Zinc Oxide 21%, 2.1 oz (62g) per bottle, Distributed by: VitaTienda Co U.S.A., San Juan, PR 00646. NDC: 35192-050-17, UPC 6 7229 99913 8
Category
Drug
Distribution
5 states
ModerateFDA (Drugs)·D-0188-2026·2025-12-03
Menthol arnica gel recalled over current good manufacturing practice deviations
CA Botana International is recalling 810 tubes of Doctor D. Schwab Clinical Weh Weh Natural Pain Relief Gel with Menthol and Arnica for CGMP deviations.
Product
Doctor D. Schwab Clinical Weh Weh Natural Pain Relief Gel with Menthol and Arnica, Menthol 5%, 4.2 oz./120 g per tube, Doctor D. Schwab, A division of CA BOTANA, San Diego, CA 92121. NDC: 35192-020-02
Category
Drug
Distribution
5 states
ModerateFDA (Drugs)·D-0193-2026·2025-12-03
Mineral sunscreen recalled over current good manufacturing practice deviations
CA Botana International is recalling 3,295 bottles of Elixir by Coco March Mineral Sunscreen SPF 50 for CGMP deviations.
Product
Elixir by Coco March Mineral Sunscreen SPF 50, Zinc Oxide 21%, 2.1 oz (62g) per bottle, Distributed by: VitaTienda Co U.S.A., San Juan, PR 00646. NDC: 35192-048-17, UPC 8 10145 82007 0
Category
Drug
Distribution
5 states
ModerateFDA (Devices)·Z-0581-2026·2025-12-03
Vitrectomy probe packs recalled with no reason stated in the record
Alcon Research is recalling 28,323 Constellation UltraVit 10K and HyperVit 20K vitrectomy probe packs; the enforcement record does not state a reason.
Product
CONSTELLATION ULTRAVIT 10K and CONSTELLATION HYPERVIT 20K, Description/REF: 25+ TOTALPLUS CP PAK 20K CPM BWV .9 IU/ 8065000093; 25+ TOTALPLUS CP PAK 20K CPM BV .9 IU/ 8065000095; 27+ TOTALPLUS CP PAK 20K CPM BV .9 IU/ 8065000096; 23GA BEVEL ULTRAVIT 10,000 CPM/ 8065752413; 25+ B
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0185-2026·2025-12-03
Tea tree balm recalled over current good manufacturing practice deviations
CA Botana International is recalling 555 tubes of Doctor D. Schwab Controlling Balm with Tea Tree Oil for CGMP deviations.
Product
Doctor D. Schwab Controlling Balm with Tea Tree Oil, Salicyclic Acid 0.8%, 1 FL OZ/ 30 ML per tube, Doctor D. Schwab, A division of CA BOTANA, San Diego, CA 92123. NDC: 35192-016-05
Category
Drug
Distribution
5 states
ModerateFDA (Drugs)·D-0192-2026·2025-12-03
Tinted mineral sunscreen recalled over manufacturing practice deviations
CA Botana International is recalling 2,090 tubes of Sugared+Bronzed Tinted Mineral Sunscreen SPF 50 for CGMP deviations.
Product
Sugared+Bronzed Tinted Mineral Sunscreen SPF 50, Zinc Oxide 21%, Net WT 3.3 OZ (93 G) per tube, Dist. By: Sugared+Bronzed, 929 Montana Ave, Santa Monica, CA 90403. NDC: 35192-055-18, UPC 8 50047 92223 6
Category
Drug
Distribution
5 states
ModerateFDA (Drugs)·D-0186-2026·2025-12-03
Benzoyl peroxide cream recalled over current good manufacturing practice deviations
CA Botana International is recalling 470 tubes of Doctor D. Schwab Controlling Cream with Benzoyl Peroxide 2.7% for CGMP deviations.
Product
Doctor D. Schwab Controlling Cream, Benzoyl Peroxide 2.7%, 1 FL OZ/ 30 ML per tube, Doctor D. Schwab, A division of CA BOTANA, San Diego, CA 92123. NDC: 35192-017-05
Category
Drug
Distribution
5 states
ModerateFDA (Drugs)·D-0184-2026·2025-12-03
Tinted moisturizer SPF 50 recalled over manufacturing practice deviations
CA Botana International is recalling 1,401 tubes of Doctor D. Schwab Flawless Skin Fluid Tinted Moisturizer SPF 50 for CGMP deviations.
Product
Doctor D. Schwab Flawless Skin Fluid Tinted Moisturizer SPF 50, Zinc Oxide 21%, 2.1 oz/61 g per tube, Manufactured by CA BOTANA, San Diego, CA 92121. NDC: 35192-043-17
Category
Drug
Distribution
5 states